11-74907721-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907721
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907721
    reference: chr 11
allele count: 4173
allele frequency: 3.591283843095406e-2
allele num: 116198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.402C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.915C>T
  hgvsp: ENST00000341411.4:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1596C>T
  hgvsp: ENST00000289575.5:c.1596C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1530C>T
  hgvsp: ENST00000428359.2:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.915C>T
  hgvsp: ENST00000454962.2:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.831C>T
  hgvsp: ENST00000531756.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.423C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1248C>T
  hgvsp: ENST00000532236.1:c.1248C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1164C>T
  hgvsp: ENST00000525650.1:c.1164C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 315
genotype depth: GenotypeDepth
  all individuals: 5733
  bin: 3.25e1
  variant carriers: 562
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 22135
  bin: 2.75e1
  variant carriers: 523
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 20243
  bin: 2.25e1
  variant carriers: 418
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 1.25e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 1.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.75e1
  variant carriers: 567
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 466
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 89
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 7.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 5965
  bin: 6.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 3.75e1
  variant carriers: 1
hgvs: p.Ser532Ser
num of homozygotes: 243
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-74907721-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907721
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907721
    reference: chr 11
allele count: 1
allele frequency: 8.606000103272e-6
allele num: 116198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1530C>A
  hgvsp: ENSP00000388912.2:p.Ser510Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.915C>A
  hgvsp: ENSP00000389653.2:p.Ser305Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1248C>A
  hgvsp: ENSP00000434112.1:p.Ser416Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.831C>A
  hgvsp: ENSP00000432650.1:p.Ser277Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.402C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.423C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1164C>A
  hgvsp: ENSP00000436324.1:p.Ser388Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.915C>A
  hgvsp: ENSP00000341286.4:p.Ser305Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1596C>A
  hgvsp: ENSP00000289575.5:p.Ser532Arg
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser532Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-74907727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907727
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907727
    reference: chr 11
allele count: 1
allele frequency: 8.712319219376199e-6
allele num: 114780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+3G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+3G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+3G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+3G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+3G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+3G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+3G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+3G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+3G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1599+3G>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

11-74907734-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907734
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907734
    reference: chr 11
allele count: 1
allele frequency: 8.920447449644074e-6
allele num: 112102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+10G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+10G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+10G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+10G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+10G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+10G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+10G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+10G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+10G>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19596
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2769
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10676
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

11-74907741-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907741
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907741
    reference: chr 11
allele count: 3
allele frequency: 2.711839892972719e-5
allele num: 110626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+17G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+17G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+17G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+17G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+17G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+17G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+17G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+17G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+17G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4484
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

11-74907743-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907743
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907743
    reference: chr 11
allele count: 1
allele frequency: 9.112613679855656e-6
allele num: 109738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+19G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+19G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+19G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+19G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+19G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+19G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+19G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+19G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+19G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14368
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3759
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

11-74907756-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907756
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907756
    reference: chr 11
allele count: 1
allele frequency: 9.434140266797487e-6
allele num: 105998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+32C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+32C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+32C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+32C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+32C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+32C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+32C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+32C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+32C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6842
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8008
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6002
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

11-74907757-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907757
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907758
    reference: chr 11
allele count: 1
allele frequency: 9.511670820096258e-6
allele num: 105134
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+34dupT
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+34dupT
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+34dupT
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+34dupT
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+34dupT
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+34dupT
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+34dupT
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+34dupT
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+34dupT
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17330
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-74907764-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907764
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907764
    reference: chr 11
allele count: 1
allele frequency: 9.881618213798691e-6
allele num: 101198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+40C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+40C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+40C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+40C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+40C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+40C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+40C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+40C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+40C>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20977
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6497
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1937
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

11-74907765-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907765
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907765
    reference: chr 11
allele count: 1
allele frequency: 9.873617693522906e-6
allele num: 101280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+41T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+41T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+41T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+41T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+41T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+41T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+41T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+41T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+41T>G
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16802
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6486
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ

11-74907769-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907769
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907769
    reference: chr 11
allele count: 1
allele frequency: 1.025662064862869e-5
allele num: 97498
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+45C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+45C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+45C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+45C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+45C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+45C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+45C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+45C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+45C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20172
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3532
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7327
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6373
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

11-74907772-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907772
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907772
    reference: chr 11
allele count: 2
allele frequency: 2.085679723021733e-5
allele num: 95892
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+48G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+48G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+48G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+48G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+48G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+48G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+48G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+48G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+48G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20093
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7768
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3889
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2824
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-74907773-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74907773
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74907773
    reference: chr 11
allele count: 1
allele frequency: 1.040647699127937e-5
allele num: 96094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.918+49C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1599+49C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.426+49C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1251+49C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.918+49C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.405+49C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.834+49C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1533+49C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1167+49C>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20139
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14077
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum

11-74911219-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911219
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911219
    reference: chr 11
allele count: 1
allele frequency: 8.855513442669405e-6
allele num: 112924
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.835-50T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.406-50T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.919-50T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.621T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1168-50T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.919-50T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1534-50T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1600-50T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.427-50T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1252-50T>C
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11281
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3617
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13073
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

11-74911223-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911223
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911223
    reference: chr 11
allele count: 26
allele frequency: 2.301170056467173e-4
allele num: 112986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.919-46T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1252-46T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1534-46T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.835-46T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.625T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1168-46T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.427-46T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.919-46T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.406-46T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1600-46T>C
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6124
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11855
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11412
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5970
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13090
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 6634
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

11-74911224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911224
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911224
    reference: chr 11
allele count: 1
allele frequency: 8.854415697108148e-6
allele num: 112938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1252-45G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.626G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.427-45G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.835-45G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.919-45G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1600-45G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.919-45G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.406-45G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1168-45G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1534-45G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13063
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

11-74911227-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911227
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911227
    reference: chr 11
allele count: 2
allele frequency: 1.769629616521262e-5
allele num: 113018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1168-42C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.919-42C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1534-42C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.919-42C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.835-42C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.427-42C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.406-42C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1600-42C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.629C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1252-42C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4447
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13062
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

11-74911254-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911254
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911254
    reference: chr 11
allele count: 12
allele frequency: 1.044004802422091e-4
allele num: 114942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.835-15C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.656C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1252-15C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1534-15C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.427-15C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1168-15C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1600-15C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.406-15C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.919-15C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.919-15C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12158
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12174
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4463
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

11-74911259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911259
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911259
    reference: chr 11
allele count: 1
allele frequency: 8.650519031141869e-6
allele num: 115600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.427-10C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1168-10C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.406-10C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.919-10C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.835-10C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.661C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.919-10C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1600-10C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1252-10C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1534-10C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13063
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

11-74911262-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911262
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911262
    reference: chr 11
allele count: 2
allele frequency: 1.722178211001274e-5
allele num: 116132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.664A>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1600-7A>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.406-7A>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1252-7A>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1534-7A>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.919-7A>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.835-7A>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.919-7A>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.427-7A>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1168-7A>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
hgvs: c.1600-7A>T
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/11-74911280-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911280
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911280
    reference: chr 11
allele count: 4
allele frequency: 3.372851914936674e-5
allele num: 118594
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1611C>A
  hgvsp: ENST00000289575.5:c.1611C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.930C>A
  hgvsp: ENST00000454962.2:c.930C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.417C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.846C>A
  hgvsp: ENST00000531756.1:c.846C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1263C>A
  hgvsp: ENST00000532236.1:c.1263C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1179C>A
  hgvsp: ENST00000525650.1:c.1179C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.682C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1545C>A
  hgvsp: ENST00000428359.2:c.1545C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.930C>A
  hgvsp: ENST00000341411.4:c.930C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.438C>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12247
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19671
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr537Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-74911280-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911280
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911280
    reference: chr 11
allele count: 1
allele frequency: 8.432129787341686e-6
allele num: 118594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.682C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1263C>T
  hgvsp: ENST00000532236.1:c.1263C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.846C>T
  hgvsp: ENST00000531756.1:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1611C>T
  hgvsp: ENST00000289575.5:c.1611C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.930C>T
  hgvsp: ENST00000454962.2:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.417C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1545C>T
  hgvsp: ENST00000428359.2:c.1545C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.930C>T
  hgvsp: ENST00000341411.4:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1179C>T
  hgvsp: ENST00000525650.1:c.1179C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.438C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12247
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr537Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

11-74911283-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911283
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911283
    reference: chr 11
allele count: 1
allele frequency: 8.403502579875292e-6
allele num: 118998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.933C>T
  hgvsp: ENST00000454962.2:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.441C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.685C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1182C>T
  hgvsp: ENST00000525650.1:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1614C>T
  hgvsp: ENST00000289575.5:c.1614C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.849C>T
  hgvsp: ENST00000531756.1:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1266C>T
  hgvsp: ENST00000532236.1:c.1266C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1548C>T
  hgvsp: ENST00000428359.2:c.1548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.933C>T
  hgvsp: ENST00000341411.4:c.933C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.420C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6143
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12269
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn538Asn
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

11-74911284-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911284
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911284
    reference: chr 11
allele count: 1
allele frequency: 8.394614015647561e-6
allele num: 119124
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1549T>G
  hgvsp: ENSP00000388912.2:p.Cys517Gly
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1183T>G
  hgvsp: ENSP00000436324.1:p.Cys395Gly
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1615T>G
  hgvsp: ENSP00000289575.5:p.Cys539Gly
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.421T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1267T>G
  hgvsp: ENSP00000434112.1:p.Cys423Gly
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.934T>G
  hgvsp: ENSP00000389653.2:p.Cys312Gly
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.686T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.850T>G
  hgvsp: ENSP00000432650.1:p.Cys284Gly
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.934T>G
  hgvsp: ENSP00000341286.4:p.Cys312Gly
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.442T>G
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys539Gly
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

11-74911292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911292
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911292
    reference: chr 11
allele count: 2
allele frequency: 1.66725020423815e-5
allele num: 119958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.858C>T
  hgvsp: ENST00000531756.1:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1191C>T
  hgvsp: ENST00000525650.1:c.1191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.694C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.450C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.942C>T
  hgvsp: ENST00000454962.2:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1275C>T
  hgvsp: ENST00000532236.1:c.1275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.942C>T
  hgvsp: ENST00000341411.4:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1557C>T
  hgvsp: ENST00000428359.2:c.1557C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1623C>T
  hgvsp: ENST00000289575.5:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.429C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5035
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys541Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

11-74911293-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911293
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911293
    reference: chr 11
allele count: 182
allele frequency: 1.515025389161741e-3
allele num: 120130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1558G>A
  hgvsp: ENSP00000388912.2:p.Val520Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.430G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1624G>A
  hgvsp: ENSP00000289575.5:p.Val542Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.695G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.943G>A
  hgvsp: ENSP00000341286.4:p.Val315Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1192G>A
  hgvsp: ENSP00000436324.1:p.Val398Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1276G>A
  hgvsp: ENSP00000434112.1:p.Val426Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.451G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.859G>A
  hgvsp: ENSP00000432650.1:p.Val287Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.943G>A
  hgvsp: ENSP00000389653.2:p.Val315Met
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9195
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10738
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12285
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val542Met
num of homozygotes: 1
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/11-74911307-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911307
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911307
    reference: chr 11
allele count: 34
allele frequency: 2.813405047579644e-4
allele num: 120850
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1206C>A
  hgvsp: ENSP00000436324.1:p.Asn402Lys
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1638C>A
  hgvsp: ENSP00000289575.5:p.Asn546Lys
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.873C>A
  hgvsp: ENSP00000432650.1:p.Asn291Lys
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.957C>A
  hgvsp: ENSP00000341286.4:p.Asn319Lys
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.957C>A
  hgvsp: ENSP00000389653.2:p.Asn319Lys
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1572C>A
  hgvsp: ENSP00000388912.2:p.Asn524Lys
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1290C>A
  hgvsp: ENSP00000434112.1:p.Asn430Lys
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.444C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.465C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.709C>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6140
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn546Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/11-74911309-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911309
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911309
    reference: chr 11
allele count: 2
allele frequency: 1.653958750268768e-5
allele num: 120922
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.959C>A
  hgvsp: ENSP00000389653.2:p.Pro320His
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.711C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.959C>A
  hgvsp: ENSP00000341286.4:p.Pro320His
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1640C>A
  hgvsp: ENSP00000289575.5:p.Pro547His
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.467C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.446C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1208C>A
  hgvsp: ENSP00000436324.1:p.Pro403His
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.875C>A
  hgvsp: ENSP00000432650.1:p.Pro292His
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1574C>A
  hgvsp: ENSP00000388912.2:p.Pro525His
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1292C>A
  hgvsp: ENSP00000434112.1:p.Pro431His
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3114
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro547His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum

11-74911309-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911309
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911309
    reference: chr 11
allele count: 2
allele frequency: 1.653958750268768e-5
allele num: 120922
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1292C>G
  hgvsp: ENSP00000434112.1:p.Pro431Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.959C>G
  hgvsp: ENSP00000341286.4:p.Pro320Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.467C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1640C>G
  hgvsp: ENSP00000289575.5:p.Pro547Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1574C>G
  hgvsp: ENSP00000388912.2:p.Pro525Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.446C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.959C>G
  hgvsp: ENSP00000389653.2:p.Pro320Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1208C>G
  hgvsp: ENSP00000436324.1:p.Pro403Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.875C>G
  hgvsp: ENSP00000432650.1:p.Pro292Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.711C>G
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7214
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro547Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

11-74911310-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911310
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911310
    reference: chr 11
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1575C>G
  hgvsp: ENST00000428359.2:c.1575C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.960C>G
  hgvsp: ENST00000341411.4:c.960C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.960C>G
  hgvsp: ENST00000454962.2:c.960C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1641C>G
  hgvsp: ENST00000289575.5:c.1641C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.876C>G
  hgvsp: ENST00000531756.1:c.876C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1293C>G
  hgvsp: ENST00000532236.1:c.1293C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.468C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1209C>G
  hgvsp: ENST00000525650.1:c.1209C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.712C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.447C>G
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5038
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro547Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

11-74911310-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911310
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911310
    reference: chr 11
allele count: 2
allele frequency: 1.653685237551884e-5
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1209C>T
  hgvsp: ENST00000525650.1:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.712C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.447C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1293C>T
  hgvsp: ENST00000532236.1:c.1293C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.960C>T
  hgvsp: ENST00000341411.4:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1641C>T
  hgvsp: ENST00000289575.5:c.1641C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.960C>T
  hgvsp: ENST00000454962.2:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1575C>T
  hgvsp: ENST00000428359.2:c.1575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.876C>T
  hgvsp: ENST00000531756.1:c.876C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.468C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro547Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

11-74911311-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911311
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911311
    reference: chr 11
allele count: 29
allele frequency: 2.397209317704631e-4
allele num: 120974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.961G>A
  hgvsp: ENSP00000341286.4:p.Val321Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1642G>A
  hgvsp: ENSP00000289575.5:p.Val548Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1210G>A
  hgvsp: ENSP00000436324.1:p.Val404Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1576G>A
  hgvsp: ENSP00000388912.2:p.Val526Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.877G>A
  hgvsp: ENSP00000432650.1:p.Val293Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.469G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.713G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1294G>A
  hgvsp: ENSP00000434112.1:p.Val432Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.961G>A
  hgvsp: ENSP00000389653.2:p.Val321Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.448G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13426
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val548Met
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

11-74911315-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911315
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911315
    reference: chr 11
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1646T>C
  hgvsp: ENSP00000289575.5:p.Leu549Pro
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.881T>C
  hgvsp: ENSP00000432650.1:p.Leu294Pro
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.965T>C
  hgvsp: ENSP00000341286.4:p.Leu322Pro
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1214T>C
  hgvsp: ENSP00000436324.1:p.Leu405Pro
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.473T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1298T>C
  hgvsp: ENSP00000434112.1:p.Leu433Pro
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.965T>C
  hgvsp: ENSP00000389653.2:p.Leu322Pro
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.717T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1580T>C
  hgvsp: ENSP00000388912.2:p.Leu527Pro
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.452T>C
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu549Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-74911321-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911321
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911321
    reference: chr 11
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.887G>T
  hgvsp: ENSP00000432650.1:p.Gly296Val
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1220G>T
  hgvsp: ENSP00000436324.1:p.Gly407Val
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1586G>T
  hgvsp: ENSP00000388912.2:p.Gly529Val
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.458G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1652G>T
  hgvsp: ENSP00000289575.5:p.Gly551Val
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.479G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.723G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.971G>T
  hgvsp: ENSP00000341286.4:p.Gly324Val
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.971G>T
  hgvsp: ENSP00000389653.2:p.Gly324Val
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1304G>T
  hgvsp: ENSP00000434112.1:p.Gly435Val
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6141
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly551Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/11-74911328-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911328
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911328
    reference: chr 11
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.486C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1227C>A
  hgvsp: ENSP00000436324.1:p.Cys409Ter
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1593C>A
  hgvsp: ENSP00000388912.2:p.Cys531Ter
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.894C>A
  hgvsp: ENSP00000432650.1:p.Cys298Ter
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1311C>A
  hgvsp: ENSP00000434112.1:p.Cys437Ter
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1659C>A
  hgvsp: ENSP00000289575.5:p.Cys553Ter
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.465C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.978C>A
  hgvsp: ENSP00000341286.4:p.Cys326Ter
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.978C>A
  hgvsp: ENSP00000389653.2:p.Cys326Ter
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.730C>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys553Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-74911328-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911328
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911328
    reference: chr 11
allele count: 3
allele frequency: 2.476964232636481e-5
allele num: 121116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.978C>T
  hgvsp: ENST00000341411.4:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1593C>T
  hgvsp: ENST00000428359.2:c.1593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.486C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1311C>T
  hgvsp: ENST00000532236.1:c.1311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1659C>T
  hgvsp: ENST00000289575.5:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.465C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.894C>T
  hgvsp: ENST00000531756.1:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.978C>T
  hgvsp: ENST00000454962.2:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1227C>T
  hgvsp: ENST00000525650.1:c.1227C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.730C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys553Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

11-74911336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911336
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911336
    reference: chr 11
allele count: 14
allele frequency: 1.155878467635403e-4
allele num: 121120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.494C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.473C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1601C>T
  hgvsp: ENSP00000388912.2:p.Thr534Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1235C>T
  hgvsp: ENSP00000436324.1:p.Thr412Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1667C>T
  hgvsp: ENSP00000289575.5:p.Thr556Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1319C>T
  hgvsp: ENSP00000434112.1:p.Thr440Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.902C>T
  hgvsp: ENSP00000432650.1:p.Thr301Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.986C>T
  hgvsp: ENSP00000341286.4:p.Thr329Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.986C>T
  hgvsp: ENSP00000389653.2:p.Thr329Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.738C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6140
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13030
  bin: 9.75e1
  variant carriers: 14
hgvs: p.Thr556Met
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD

11-74911337-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911337
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911337
    reference: chr 11
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1236G>A
  hgvsp: ENST00000525650.1:c.1236G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.987G>A
  hgvsp: ENST00000341411.4:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.903G>A
  hgvsp: ENST00000531756.1:c.903G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1668G>A
  hgvsp: ENST00000289575.5:c.1668G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.987G>A
  hgvsp: ENST00000454962.2:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1602G>A
  hgvsp: ENST00000428359.2:c.1602G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1320G>A
  hgvsp: ENST00000532236.1:c.1320G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.739G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.495G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.474G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr556Thr
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

11-74911353-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911353
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911353
    reference: chr 11
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1003G>A
  hgvsp: ENSP00000341286.4:p.Val335Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.919G>A
  hgvsp: ENSP00000432650.1:p.Val307Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1003G>A
  hgvsp: ENSP00000389653.2:p.Val335Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.511G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1336G>A
  hgvsp: ENSP00000434112.1:p.Val446Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1684G>A
  hgvsp: ENSP00000289575.5:p.Val562Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.490G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1618G>A
  hgvsp: ENSP00000388912.2:p.Val540Met
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.755G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1252G>A
  hgvsp: ENSP00000436324.1:p.Val418Met
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12370
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2267
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3601
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val562Met
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

11-74911358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911358
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911358
    reference: chr 11
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1689C>T
  hgvsp: ENST00000289575.5:c.1689C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.516C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1257C>T
  hgvsp: ENST00000525650.1:c.1257C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1341C>T
  hgvsp: ENST00000532236.1:c.1341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1008C>T
  hgvsp: ENST00000341411.4:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1623C>T
  hgvsp: ENST00000428359.2:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.924C>T
  hgvsp: ENST00000531756.1:c.924C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.495C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1008C>T
  hgvsp: ENST00000454962.2:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.760C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5036
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro563Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

11-74911373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911373
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911373
    reference: chr 11
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1356C>T
  hgvsp: ENST00000532236.1:c.1356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1023C>T
  hgvsp: ENST00000454962.2:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1638C>T
  hgvsp: ENST00000428359.2:c.1638C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.939C>T
  hgvsp: ENST00000531756.1:c.939C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.510C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1023C>T
  hgvsp: ENST00000341411.4:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1704C>T
  hgvsp: ENST00000289575.5:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1272C>T
  hgvsp: ENST00000525650.1:c.1272C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.775C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.531C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3601
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val568Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

11-74911379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911379
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911379
    reference: chr 11
allele count: 1
allele frequency: 8.276775368316504e-6
allele num: 120820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.945G>A
  hgvsp: ENST00000531756.1:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1644G>A
  hgvsp: ENST00000428359.2:c.1644G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.781G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.516G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1029G>A
  hgvsp: ENST00000341411.4:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1278G>A
  hgvsp: ENST00000525650.1:c.1278G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1362G>A
  hgvsp: ENST00000532236.1:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1710G>A
  hgvsp: ENST00000289575.5:c.1710G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.537G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1029G>A
  hgvsp: ENST00000454962.2:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu570Leu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

11-74911384-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911384
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911384
    reference: chr 11
allele count: 1
allele frequency: 8.291598951941893e-6
allele num: 120604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.542C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.950C>G
  hgvsp: ENSP00000432650.1:p.Ser317Trp
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1283C>G
  hgvsp: ENSP00000436324.1:p.Ser428Trp
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1649C>G
  hgvsp: ENSP00000388912.2:p.Ser550Trp
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.786C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1367C>G
  hgvsp: ENSP00000434112.1:p.Ser456Trp
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1715C>G
  hgvsp: ENSP00000289575.5:p.Ser572Trp
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1034C>G
  hgvsp: ENSP00000389653.2:p.Ser345Trp
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.521C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1034C>G
  hgvsp: ENSP00000341286.4:p.Ser345Trp
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7132
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser572Trp
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

11-74911385-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911385
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911385
    reference: chr 11
allele count: 8
allele frequency: 6.634599436059048e-5
allele num: 120580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1368G>A
  hgvsp: ENST00000532236.1:c.1368G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.522G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.951G>A
  hgvsp: ENST00000531756.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1650G>A
  hgvsp: ENST00000428359.2:c.1650G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1284G>A
  hgvsp: ENST00000525650.1:c.1284G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1716G>A
  hgvsp: ENST00000289575.5:c.1716G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.543G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.787G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1035G>A
  hgvsp: ENST00000341411.4:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1035G>A
  hgvsp: ENST00000454962.2:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser572Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

11-74911394-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911394
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911394
    reference: chr 11
allele count: 1
allele frequency: 8.326256015719971e-6
allele num: 120102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1044C>T
  hgvsp: ENST00000454962.2:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1377C>T
  hgvsp: ENST00000532236.1:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1293C>T
  hgvsp: ENST00000525650.1:c.1293C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1044C>T
  hgvsp: ENST00000341411.4:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.552C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.531C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1659C>T
  hgvsp: ENST00000428359.2:c.1659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1725C>T
  hgvsp: ENST00000289575.5:c.1725C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.960C>T
  hgvsp: ENST00000531756.1:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.796C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala575Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

11-74911397-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911397
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911397
    reference: chr 11
allele count: 129
allele frequency: 1.075286743131502e-3
allele num: 119968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.799T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1662T>C
  hgvsp: ENST00000428359.2:c.1662T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1380T>C
  hgvsp: ENST00000532236.1:c.1380T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1296T>C
  hgvsp: ENST00000525650.1:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1047T>C
  hgvsp: ENST00000341411.4:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1728T>C
  hgvsp: ENST00000289575.5:c.1728T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.534T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.555T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.963T>C
  hgvsp: ENST00000531756.1:c.963T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1047T>C
  hgvsp: ENST00000454962.2:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9194
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13167
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9731
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.75e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 1295
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys576Cys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-74911403-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911403
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911403
    reference: chr 11
allele count: 1
allele frequency: 8.368480953337351e-6
allele num: 119496
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1734C>T
  hgvsp: ENST00000289575.5:c.1734C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1302C>T
  hgvsp: ENST00000525650.1:c.1302C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.969C>T
  hgvsp: ENST00000531756.1:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.805C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.561C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1053C>T
  hgvsp: ENST00000341411.4:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1668C>T
  hgvsp: ENST00000428359.2:c.1668C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1386C>T
  hgvsp: ENST00000532236.1:c.1386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1053C>T
  hgvsp: ENST00000454962.2:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.540C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr578Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

11-74911412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911412
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911412
    reference: chr 11
allele count: 1
allele frequency: 8.457947087083023e-6
allele num: 118232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1062C>T
  hgvsp: ENST00000341411.4:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1743C>T
  hgvsp: ENST00000289575.5:c.1743C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1311C>T
  hgvsp: ENST00000525650.1:c.1311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.549C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1677C>T
  hgvsp: ENST00000428359.2:c.1677C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1062C>T
  hgvsp: ENST00000454962.2:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1395C>T
  hgvsp: ENST00000532236.1:c.1395C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.978C>T
  hgvsp: ENST00000531756.1:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.814C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.570C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4980
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro581Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

11-74911414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911414
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911414
    reference: chr 11
allele count: 2
allele frequency: 1.691818366380186e-5
allele num: 118216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.572C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1313C>T
  hgvsp: ENSP00000436324.1:p.Ser438Phe
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.816C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1064C>T
  hgvsp: ENSP00000389653.2:p.Ser355Phe
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1064C>T
  hgvsp: ENSP00000341286.4:p.Ser355Phe
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1745C>T
  hgvsp: ENSP00000289575.5:p.Ser582Phe
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.980C>T
  hgvsp: ENSP00000432650.1:p.Ser327Phe
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.551C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1679C>T
  hgvsp: ENSP00000388912.2:p.Ser560Phe
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1397C>T
  hgvsp: ENSP00000434112.1:p.Ser466Phe
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6130
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12960
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser582Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

11-74911420-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911420
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911420
    reference: chr 11
allele count: 1
allele frequency: 8.49733183780293e-6
allele num: 117684
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1751T>G
  hgvsp: ENSP00000289575.5:p.Met584Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1403T>G
  hgvsp: ENSP00000434112.1:p.Met468Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.557T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.578T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1319T>G
  hgvsp: ENSP00000436324.1:p.Met440Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1070T>G
  hgvsp: ENSP00000389653.2:p.Met357Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1070T>G
  hgvsp: ENSP00000341286.4:p.Met357Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1685T>G
  hgvsp: ENSP00000388912.2:p.Met562Arg
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.822T>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.986T>G
  hgvsp: ENSP00000432650.1:p.Met329Arg
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met584Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-74911443-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911443
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911443
    reference: chr 11
allele count: 5
allele frequency: 4.353125544140693e-5
allele num: 114860
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.580G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+11G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+11G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+11G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+11G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+11G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+11G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.845G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+11G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+11G>C
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-74911444-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911444
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911444
    reference: chr 11
allele count: 1
allele frequency: 8.710042679209128e-6
allele num: 114810
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+12G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+12G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+12G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.846G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+12G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.581G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+12G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+12G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+12G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+12G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4844
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

11-74911444-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911444
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911444
    reference: chr 11
allele count: 1
allele frequency: 8.710042679209128e-6
allele num: 114810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+12G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+12G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+12G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+12G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000528108
  gene symbol: SLCO2B1
  hgvsc: ENST00000528108.1:n.581G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+12G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+12G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.846G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+12G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+12G>T
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4948
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2953
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-74911446-T-TGGGGAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911446
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911452
    reference: chr 11
allele count: 1
allele frequency: 8.727526618956187e-6
allele num: 114580
alternate allele: TGGGGAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+18_1331+19insAAGGGG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+18_1697+19insAAGGGG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+18_590+19insAAGGGG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+18_1763+19insAAGGGG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.852_853insAAGGGG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+18_998+19insAAGGGG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+18_1415+19insAAGGGG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+18_1082+19insAAGGGG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+18_1082+19insAAGGGG
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6469
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12955
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

11-74911446-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911446
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911445
    reference: chr 11
allele count: 10
allele frequency: 8.727526618956188e-5
allele num: 114580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+18delG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+18delG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+18delG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.852delG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+18delG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+18delG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+18delG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+18delG
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+18delG
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6469
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4958
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2941
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: TG
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

11-74911455-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911455
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911455
    reference: chr 11
allele count: 2
allele frequency: 1.761307594758349e-5
allele num: 113552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+23G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+23G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+23G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+23G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.857G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+23G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+23G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+23G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+23G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6375
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3596
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

11-74911459-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911459
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911459
    reference: chr 11
allele count: 61
allele frequency: 5.402437296301545e-4
allele num: 112912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.861G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+27G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+27G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+27G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+27G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+27G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+27G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+27G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+27G>T
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11622
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9079
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10993
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4888
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

11-74911465-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911465
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911465
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 112066
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+33T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+33T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.867T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+33T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+33T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+33T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+33T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+33T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+33T>C
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9061
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4416
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2910
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum

11-74911467-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911467
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911467
    reference: chr 11
allele count: 8
allele frequency: 7.162938953852766e-5
allele num: 111686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+35C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+35C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+35C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+35C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+35C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.869C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+35C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+35C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+35C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11491
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9058
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10552
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4284
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

11-74911474-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74911474
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74911474
    reference: chr 11
allele count: 1
allele frequency: 9.011931797700155e-6
allele num: 110964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1415+42G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.590+42G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1331+42G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1082+42G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1697+42G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.998+42G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.876G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1763+42G>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1082+42G>T
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11213
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12916
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11729
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

11-74913899-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74913899
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74913899
    reference: chr 11
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.3301G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.999-47G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1416-47G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1332-47G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1083-47G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1764-47G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.591-47G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1698-47G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1083-47G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3195
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3124
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5109
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3332
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

11-74913900-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74913900
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74913900
    reference: chr 11
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.999-46G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1416-46G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1764-46G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.591-46G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1083-46G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1698-46G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.3302G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1332-46G>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1083-46G>A
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7055
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38307
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3335
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

11-74913917-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74913917
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74913917
    reference: chr 11
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1083-29C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.591-29C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1083-29C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.999-29C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.3319C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1332-29C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1698-29C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1764-29C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1416-29C>G
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5701
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38299
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-74913925-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74913925
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74913925
    reference: chr 11
allele count: 33
allele frequency: 2.71891375276011e-4
allele num: 121372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.3327G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.999-21G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1764-21G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1698-21G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.591-21G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1083-21G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1083-21G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1332-21G>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1416-21G>C
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6352
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3433
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

11-74913928-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74913928
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74913928
    reference: chr 11
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.3330C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1083-18C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1083-18C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1416-18C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.999-18C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1332-18C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.591-18C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1698-18C>T
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1764-18C>T
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/11-74913933-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74913933
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74913933
    reference: chr 11
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.3335C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1764-13C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1332-13C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1083-13C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1083-13C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.591-13C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1698-13C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.999-13C>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1416-13C>A
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3191
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

11-74913933-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74913933
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74913933
    reference: chr 11
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.3335C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1416-13C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1698-13C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.591-13C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1083-13C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.999-13C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1764-13C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1083-13C>G
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1332-13C>G
  variant of: http://identifiers.org/hgnc/10962
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP

11-74913940-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74913940
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74913940
    reference: chr 11
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.999-6T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1332-6T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1764-6T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1083-6T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.3342T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1083-6T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.591-6T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1698-6T>C
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1416-6T>C
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5919
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1764-6T>C
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

11-74913942-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74913942
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 74913942
    reference: chr 11
allele count: 6
allele frequency: 4.942339373970346e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000388912
  ensembl transcript: ENST00000428359
  gene symbol: SLCO2B1
  hgvsc: ENST00000428359.2:c.1698-4T>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000341286
  ensembl transcript: ENST00000341411
  gene symbol: SLCO2B1
  hgvsc: ENST00000341411.4:c.1083-4T>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000289575
  ensembl transcript: ENST00000289575
  gene symbol: SLCO2B1
  hgvsc: ENST00000289575.5:c.1764-4T>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530015
  gene symbol: SLCO2B1
  hgvsc: ENST00000530015.1:n.3344T>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000389653
  ensembl transcript: ENST00000454962
  gene symbol: SLCO2B1
  hgvsc: ENST00000454962.2:c.1083-4T>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000432650
  ensembl transcript: ENST00000531756
  gene symbol: SLCO2B1
  hgvsc: ENST00000531756.1:c.999-4T>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000436324
  ensembl transcript: ENST00000525650
  gene symbol: SLCO2B1
  hgvsc: ENST00000525650.1:c.1332-4T>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl transcript: ENST00000530012
  gene symbol: SLCO2B1
  hgvsc: ENST00000530012.1:n.591-4T>A
  variant of: http://identifiers.org/hgnc/10962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137491
  ensembl protein: ENSP00000434112
  ensembl transcript: ENST00000532236
  gene symbol: SLCO2B1
  hgvsc: ENST00000532236.1:c.1416-4T>A
  variant of: http://identifiers.org/hgnc/10962
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: c.1764-4T>A
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum

GenotypeQuality
all individuals: 115
bin: 8.75e1
variant carriers: 15

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 4

GenotypeQuality
all individuals: 38111
bin: 6.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1208
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 846
bin: 7.75e1
variant carriers: 24

GenotypeQuality
all individuals: 252
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 233
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 22

GenotypeQuality
all individuals: 5216
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 23

GenotypeQuality
all individuals: 4589
bin: 9.75e1
variant carriers: 3779

GenotypeQuality
all individuals: 1192
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 390
bin: 5.25e1
variant carriers: 10

European (Finnish)
type: Population
allele count: 208
allele frequency: 3.301587301587302e-2
allele num: 6300
num of homozygotes: 5

East Asian
type: Population
allele count: 237
allele frequency: 2.788891503883267e-2
allele num: 8498
num of homozygotes: 9

Other
type: Population
allele count: 32
allele frequency: 3.782505910165485e-2
allele num: 846
num of homozygotes: 1

South Asian
type: Population
allele count: 245
allele frequency: 1.664628346242696e-2
allele num: 14718
num of homozygotes: 5

African
type: Population
allele count: 2043
allele frequency: 2.022371807562859e-1
allele num: 10102
num of homozygotes: 212

Latino
type: Population
allele count: 148
allele frequency: 1.306497175141243e-2
allele num: 11328
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1260
allele frequency: 1.956339471477813e-2
allele num: 64406
num of homozygotes: 10

BaseQRankSum
type: SiteQuality
SIO_000300: -1.849e0

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

FS
type: SiteQuality
SIO_000300: 7.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.64e-2

QD
type: SiteQuality
SIO_000300: 1.501e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.84e-1

DP
type: SiteQuality
SIO_000300: 1.518705e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

GenotypeQuality
all individuals: 252
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5216
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4589
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 390
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14718
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55265037418874e-5
allele num: 64406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.64e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

DP
type: SiteQuality
SIO_000300: 1.518705e6

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

FS
type: SiteQuality
SIO_000300: 7.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.849e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

QD
type: SiteQuality
SIO_000300: 1.501e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 267
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38624
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7003
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 738
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.184834123222749e-4
allele num: 8440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.161e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.430347e6

FS
type: SiteQuality
SIO_000300: 5.715e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.046e0

QD
type: SiteQuality
SIO_000300: 5.91e0

GenotypeQuality
all individuals: 761
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31096
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 471
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6046
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.286505392013991e-5
allele num: 13724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11006
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.623e0

VQSLOD
type: SiteQuality
SIO_000300: -1.139e0

DP
type: SiteQuality
SIO_000300: 1.334317e6

QD
type: SiteQuality
SIO_000300: 6.16e0

GenotypeQuality
all individuals: 488
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12914
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3469
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1862
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.616344475334583e-5
allele num: 61868
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.051745898190997e-4
allele num: 9508
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.470491558344539e-5
allele num: 13386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10882
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e0

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

DP
type: SiteQuality
SIO_000300: 1.273054e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

QD
type: SiteQuality
SIO_000300: 1.38e1

GenotypeQuality
all individuals: 592
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4073
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13216
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5944
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.225790634959549e-4
allele num: 8158
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61402
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.258e0

InbreedingCoeff
type: SiteQuality
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MQ
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SIO_000300: 5.9e1

BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -9.499e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.224773e6

QD
type: SiteQuality
SIO_000300: 1.23e1

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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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7880
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.172605426610003e-5
allele num: 12236
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10540
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5710
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59762
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.981e0

QD
type: SiteQuality
SIO_000300: 6.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.095e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59322
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12114
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.281394156842645e-4
allele num: 7804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5658
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.045731e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.241e0

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.068e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

MQ
type: SiteQuality
SIO_000300: 6.028e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.742767514813524e-5
allele num: 57380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5402
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e0

VQSLOD
type: SiteQuality
SIO_000300: -1.908e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.898e0

MQ
type: SiteQuality
SIO_000300: 5.744e1

DP
type: SiteQuality
SIO_000300: 9.8012e5

QD
type: SiteQuality
SIO_000300: 8.98e0

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: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57416
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.692628650904033e-5
allele num: 11504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5400
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.766e0

VQSLOD
type: SiteQuality
SIO_000300: -1.229e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

QD
type: SiteQuality
SIO_000300: 1.706e1

FS
type: SiteQuality
SIO_000300: 4.15e0

DP
type: SiteQuality
SIO_000300: 9.79056e5

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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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.130752373995617e-5
allele num: 10952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55350
num of homozygotes: 0

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

Latino
type: Population
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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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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
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.672285263119239e-5
allele num: 54462
num of homozygotes: 0

East Asian
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 1.831568921938533e-5
allele num: 54598
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

African
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Other
type: Population
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.552795031055901e-5
allele num: 64400
num of homozygotes: 0

FS
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MQ
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: -2.209e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 1.933098e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

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: 0

GenotypeQuality
all individuals: 116
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

South Asian
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allele count: 26
allele frequency: 2.35934664246824e-3
allele num: 11020
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.938872e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

QD
type: SiteQuality
SIO_000300: 1.389e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

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
all individuals: 211
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.097525473071325e-5
allele num: 10992
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.940274e6

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.427e0

FS
type: SiteQuality
SIO_000300: 2.095e0

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.015e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.538e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.869e1

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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

South Asian
type: Population
allele count: 2
allele frequency: 1.813236627379873e-4
allele num: 11030
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64422
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 3.041e0

DP
type: SiteQuality
SIO_000300: 1.945041e6

QD
type: SiteQuality
SIO_000300: 1.098e1

GenotypeQuality
all individuals: 17326
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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: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537609939110646e-5
allele num: 65036
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.07128944292949e-3
allele num: 10268
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.919e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.346e1

DP
type: SiteQuality
SIO_000300: 1.979629e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.985e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 17762
bin: 6.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.721952167995334e-5
allele num: 10286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65204
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.311e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e-1

FS
type: SiteQuality
SIO_000300: 3.14e0

QD
type: SiteQuality
SIO_000300: 1.407e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.985593e6

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65348
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.554726368159204e-4
allele num: 12864
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.989926e6

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.629e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.548762736535663e-5
allele num: 65952
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14584
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.136363636363636e-3
allele num: 880
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

DP
type: SiteQuality
SIO_000300: 2.01725e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.308e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

QD
type: SiteQuality
SIO_000300: 1.35e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-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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variant carriers: 1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65952
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.856829402084476e-5
allele num: 14584
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

DP
type: SiteQuality
SIO_000300: 2.01725e6

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

FS
type: SiteQuality
SIO_000300: 3.308e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13061
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.128668171557562e-3
allele num: 886
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: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66060
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.567e0

DP
type: SiteQuality
SIO_000300: 2.021448e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.113e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.253e0

MQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

QD
type: SiteQuality
SIO_000300: 1.099e1

VQSLOD
type: SiteQuality
SIO_000300: 8.75e-1

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66098
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: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14940
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.862e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.31e-1

QD
type: SiteQuality
SIO_000300: 1.016e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.102e0

DP
type: SiteQuality
SIO_000300: 2.022506e6

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508705229172324e-5
allele num: 66282
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15570
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 2.032951e6

QD
type: SiteQuality
SIO_000300: 1.206e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.73e-1

FS
type: SiteQuality
SIO_000300: 4.574e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.421e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7129
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variant carriers: 0

GenotypeQuality
all individuals: 13149
bin: 9.75e1
variant carriers: 181

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.889616644191871e-4
allele num: 10382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 171
allele frequency: 2.578329965923826e-3
allele num: 66322
num of homozygotes: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058681185722928e-3
allele num: 6612
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
SIO_000300: 4.05e0

FS
type: SiteQuality
SIO_000300: 5.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.92e-1

QD
type: SiteQuality
SIO_000300: 1.316e1

DP
type: SiteQuality
SIO_000300: 2.047098e6

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 34

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3115
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variant carriers: 0

GenotypeQuality
all individuals: 4479
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.1667488899852e-5
allele num: 16216
num of homozygotes: 0

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

African
type: Population
allele count: 32
allele frequency: 3.081664098613251e-3
allele num: 10384
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: -1.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.045748e6

FS
type: SiteQuality
SIO_000300: 2.726e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.955e1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.332e1

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

African
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allele count: 2
allele frequency: 1.925669170036588e-4
allele num: 10386
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 2.04694e6

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006253006253006e-5
allele num: 66528
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.932e1

BaseQRankSum
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VQSLOD
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

FS
type: SiteQuality
SIO_000300: 5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2268
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GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
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FS
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BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.399e1

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

InbreedingCoeff
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SIO_000300: 1.0e-4

DP
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SIO_000300: 2.047165e6

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

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

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

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

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

East Asian
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allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
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QD
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ClippingRankSum
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SIO_000300: -1.88e-1

FS
type: SiteQuality
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VQSLOD
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SIO_000300: 6.38e-1

BaseQRankSum
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SIO_000300: 2.12e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.133464180569185e-5
allele num: 16304
num of homozygotes: 0

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

European (Finnish)
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allele count: 2
allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 26
allele frequency: 3.907071799957924e-4
allele num: 66546
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.620000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

MQRankSum
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SIO_000300: 3.02e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

QD
type: SiteQuality
SIO_000300: 1.193e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.049888e6

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.785e0

MQRankSum
type: SiteQuality
SIO_000300: -1.393e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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SIO_000300: 2.048121e6

BaseQRankSum
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SIO_000300: -3.871e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
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

BaseQRankSum
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SIO_000300: -1.44e0

QD
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.94e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.542e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

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

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

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

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

Other
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num of homozygotes: 0

East Asian
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allele frequency: 1.156871818602499e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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South Asian
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allele count: 1
allele frequency: 6.093845216331505e-5
allele num: 16410
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

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

Latino
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East Asian
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European (Non-Finnish)
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allele frequency: 1.50195253829979e-5
allele num: 66580
num of homozygotes: 0

European (Finnish)
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allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

Other
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South Asian
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allele frequency: 7.305491294289541e-4
allele num: 16426
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MQRankSum
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DP
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.087168249330411e-5
allele num: 16428
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 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
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.049005e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.086427267194157e-5
allele num: 16430
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66568
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.98e-1

DP
type: SiteQuality
SIO_000300: 2.048076e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

QD
type: SiteQuality
SIO_000300: 7.76e0

VQSLOD
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SIO_000300: -2.029e0

FS
type: SiteQuality
SIO_000300: 1.1654e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.98e-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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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.97e-1

FS
type: SiteQuality
SIO_000300: 7.032e0

VQSLOD
type: SiteQuality
SIO_000300: 5.1e-2

BaseQRankSum
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SIO_000300: -4.208e0

DP
type: SiteQuality
SIO_000300: 2.047534e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.561e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.38e-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
all individuals: 88
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.110228522546743e-5
allele num: 16366
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: 906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.045353e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.266e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.216e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.663703131039814e-5
allele num: 10348
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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 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
allele num: 11568
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.369e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.043414e6

QD
type: SiteQuality
SIO_000300: 8.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 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
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506296318611797e-5
allele num: 66388
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 2.039514e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 1.239e1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.06e-1

GenotypeQuality
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variant carriers: 8

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.01295570955107e-5
allele num: 66380
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 902
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.855746628726958e-4
allele num: 16166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 2.040388e6

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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SIO_000300: -6.929999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.311e1

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66200
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South Asian
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allele count: 0
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Latino
type: Population
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allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

Other
type: Population
allele count: 0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: -1.821e0

VQSLOD
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FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: -2.25e0

ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 218
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13071
bin: 9.75e1
variant carriers: 129

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

GenotypeQuality
all individuals: 3593
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4992
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3054
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2261
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7064
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 120
allele frequency: 1.164144353899884e-2
allele num: 10308
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.323015735777278e-4
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.327512022272843e-5
allele num: 15804
num of homozygotes: 0

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

Other
type: Population
allele count: 3
allele frequency: 3.348214285714286e-3
allele num: 896
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 1.967e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 2.040018e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

GenotypeQuality
all individuals: 247
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12963
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3038
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4454
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4999
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GenotypeQuality
all individuals: 19609
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variant carriers: 0

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

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3602
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variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6989
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515013786625458e-5
allele num: 66006
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: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.137e0

VQSLOD
type: SiteQuality
SIO_000300: -2.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.19e0

QD
type: SiteQuality
SIO_000300: 1.42e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.25e-1

FS
type: SiteQuality
SIO_000300: 4.485e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

DP
type: SiteQuality
SIO_000300: 2.01937e6

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6809
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2993
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 207
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GenotypeQuality
all individuals: 18027
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2861
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variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3601
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12960
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14800
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
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: 8604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.064e1

VQSLOD
type: SiteQuality
SIO_000300: -1.327e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

DP
type: SiteQuality
SIO_000300: 1.996983e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.813e0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 3.505e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.256e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.56e0

GenotypeQuality
all individuals: 18218
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2903
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2991
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3601
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.050547573289405e-5
allele num: 65562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
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: 10216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.727e0

QD
type: SiteQuality
SIO_000300: 1.319e1

FS
type: SiteQuality
SIO_000300: 2.021e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

DP
type: SiteQuality
SIO_000300: 1.996675e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.62e-1

GenotypeQuality
all individuals: 17720
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4972
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12960
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
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variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4441
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6745
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2262
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529987760097919e-5
allele num: 65360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 5.942e0

VQSLOD
type: SiteQuality
SIO_000300: -4.852e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 1.986428e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

QD
type: SiteQuality
SIO_000300: 1.276e1

GenotypeQuality
all individuals: 4947
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14956
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4809
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4439
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3598
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2955
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6490
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12967
bin: 9.75e1
variant carriers: 5

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.776049766718506e-5
allele num: 64300
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13094
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.542e1

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

FS
type: SiteQuality
SIO_000300: 8.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.56e-1

DP
type: SiteQuality
SIO_000300: 1.943095e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.225e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2953
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4948
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3597
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 724
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12963
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2266
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555645437291932e-5
allele num: 64282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13068
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.83e-1

DP
type: SiteQuality
SIO_000300: 1.942718e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.09e-1

QD
type: SiteQuality
SIO_000300: 1.279e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 6.399e0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 15020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
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variant carriers: 0

GenotypeQuality
all individuals: 3597
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12963
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.691117677733357e-5
allele num: 11506
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13068
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

VQSLOD
type: SiteQuality
SIO_000300: 2.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.64e-1

FS
type: SiteQuality
SIO_000300: 6.399e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.09e-1

DP
type: SiteQuality
SIO_000300: 1.942718e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.279e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560159760359461e-5
allele num: 64096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13086
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.942958e6

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.240639041437844e-5
allele num: 64096
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.585052728106373e-4
allele num: 13086
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 1.942958e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.34852043212776e-4
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12282
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-2

DP
type: SiteQuality
SIO_000300: 1.928035e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

FS
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e-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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variant carriers: 60

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11942
num of homozygotes: 0

African
type: Population
allele count: 57
allele frequency: 5.748285599031868e-3
allele num: 9916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63670
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.489183531053733e-4
allele num: 11464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

VQSLOD
type: SiteQuality
SIO_000300: 5.6e0

QD
type: SiteQuality
SIO_000300: 1.474e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.61e0

DP
type: SiteQuality
SIO_000300: 1.921444e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.163e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.79e1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.907704e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

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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bin: 9.75e1
variant carriers: 8

Latino
type: Population
allele count: 1
allele frequency: 8.736676568233443e-5
allele num: 11446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.905388312673918e-5
allele num: 63248
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

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

Other
type: Population
allele count: 1
allele frequency: 1.25e-3
allele num: 800
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-1

FS
type: SiteQuality
SIO_000300: 2.682e0

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.457e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-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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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10948
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
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Latino
type: Population
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allele frequency: 8.751969193068441e-5
allele num: 11426
num of homozygotes: 0

Other
type: Population
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.078e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
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African
type: Population
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allele frequency: 9.611687812379854e-5
allele num: 10404
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele num: 906
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South Asian
type: Population
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allele num: 16490
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-2

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.45e-1

VQSLOD
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DP
type: SiteQuality
SIO_000300: 3.06623e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.619e0

QD
type: SiteQuality
SIO_000300: 1.285e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

GenotypeQuality
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bin: 2.75e1
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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bin: 6.75e1
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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: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.391e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.251e0

DP
type: SiteQuality
SIO_000300: 3.071917e6

FS
type: SiteQuality
SIO_000300: 1.508e0

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.485e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 9.6e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 33

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 31
allele frequency: 4.647397457423843e-4
allele num: 66704
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.477e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 5.73e0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.854e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

DP
type: SiteQuality
SIO_000300: 3.07466e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.917e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.206e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.305e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.533e1

MQRankSum
type: SiteQuality
SIO_000300: -1.389e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.073062e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2935
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variant carriers: 0

GenotypeQuality
all individuals: 1870
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

DP
type: SiteQuality
SIO_000300: 3.07335e6

QD
type: SiteQuality
SIO_000300: 1.323e1

GenotypeQuality
all individuals: 1870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

DP
type: SiteQuality
SIO_000300: 3.07335e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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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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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e0

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.073834e6

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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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994485073732166e-5
allele num: 66728
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.842e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e-3