12-131620642-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620642
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620642
    reference: chr 12
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2328C>T
  hgvsp: ENST00000261654.5:c.2328C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2533C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.885C>T
  hgvsp: ENST00000543617.1:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.368C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.389C>T
  hgvsp: ENST00000335486.6:c.389C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1386C>T
  hgvsp: ENST00000376682.4:c.1386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.195C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2424C>T
  hgvsp: ENST00000535015.1:c.2424C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3457
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly776Gly
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

12-131620643-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620643
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620643
    reference: chr 12
allele count: 38
allele frequency: 3.148614609571788e-4
allele num: 120688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.369G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.196G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2534G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1387G>A
  hgvsp: ENSP00000365872.4:p.Val463Met
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.390G>A
  hgvsp: ENSP00000334127.6:p.Val131Met
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2425G>A
  hgvsp: ENSP00000444425.1:p.Val809Met
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2329G>A
  hgvsp: ENSP00000261654.5:p.Val777Met
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.886G>A
  hgvsp: ENSP00000438021.1:p.Val296Met
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14578
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23112
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3453
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val777Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

12-131620649-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620649
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620649
    reference: chr 12
allele count: 2
allele frequency: 1.658072325114821e-5
allele num: 120622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.202G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2335G>A
  hgvsp: ENSP00000261654.5:p.Ala779Thr
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2540G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.892G>A
  hgvsp: ENSP00000438021.1:p.Ala298Thr
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2431G>A
  hgvsp: ENSP00000444425.1:p.Ala811Thr
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1393G>A
  hgvsp: ENSP00000365872.4:p.Ala465Thr
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.396G>A
  hgvsp: ENSP00000334127.6:p.Ala133Thr
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.375G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2074
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3435
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala779Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

12-131620650-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620650
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620650
    reference: chr 12
allele count: 386
allele frequency: 3.200079587471605e-3
allele num: 120622
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2432C>T
  hgvsp: ENSP00000444425.1:p.Ala811Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.376C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1394C>T
  hgvsp: ENSP00000365872.4:p.Ala465Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2336C>T
  hgvsp: ENSP00000261654.5:p.Ala779Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2541C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.893C>T
  hgvsp: ENSP00000438021.1:p.Ala298Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.397C>T
  hgvsp: ENSP00000334127.6:p.Ala133Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.203C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14543
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 23084
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 9.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 6.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3750
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31243
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala779Val
num of homozygotes: 3
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

12-131620651-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620651
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620651
    reference: chr 12
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2542T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.377T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2337T>C
  hgvsp: ENST00000261654.5:c.2337T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2433T>C
  hgvsp: ENST00000535015.1:c.2433T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.398T>C
  hgvsp: ENST00000335486.6:c.398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.894T>C
  hgvsp: ENST00000543617.1:c.894T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1395T>C
  hgvsp: ENST00000376682.4:c.1395T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.204T>C
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10638
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala779Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-131620654-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620654
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620654
    reference: chr 12
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1398C>T
  hgvsp: ENST00000376682.4:c.1398C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.207C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2436C>T
  hgvsp: ENST00000535015.1:c.2436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.401C>T
  hgvsp: ENST00000335486.6:c.401C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.897C>T
  hgvsp: ENST00000543617.1:c.897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2340C>T
  hgvsp: ENST00000261654.5:c.2340C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.380C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2545C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31363
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val780Val
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

12-131620656-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620656
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620656
    reference: chr 12
allele count: 7
allele frequency: 5.80710457765758e-5
allele num: 120542
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2342A>G
  hgvsp: ENSP00000261654.5:p.Asn781Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2438A>G
  hgvsp: ENSP00000444425.1:p.Asn813Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1400A>G
  hgvsp: ENSP00000365872.4:p.Asn467Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2547A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.209A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.899A>G
  hgvsp: ENSP00000438021.1:p.Asn300Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.403A>G
  hgvsp: ENSP00000334127.6:p.Asn135Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.382A>G
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14568
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23166
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3437
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn781Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

12-131620658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620658
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620658
    reference: chr 12
allele count: 7
allele frequency: 5.809514324602463e-5
allele num: 120492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.901G>A
  hgvsp: ENSP00000438021.1:p.Gly301Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.405G>A
  hgvsp: ENSP00000334127.6:p.Gly136Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.211G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2549G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2344G>A
  hgvsp: ENSP00000261654.5:p.Gly782Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.384G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1402G>A
  hgvsp: ENSP00000365872.4:p.Gly468Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2440G>A
  hgvsp: ENSP00000444425.1:p.Gly814Ser
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14546
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8596
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3746
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6275
  bin: 9.75e1
  variant carriers: 7
hgvs: p.Gly782Ser
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

12-131620659-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620659
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620659
    reference: chr 12
allele count: 1
allele frequency: 8.300132802124834e-6
allele num: 120480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.385G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2441G>A
  hgvsp: ENSP00000444425.1:p.Gly814Asp
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.212G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.902G>A
  hgvsp: ENSP00000438021.1:p.Gly301Asp
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2345G>A
  hgvsp: ENSP00000261654.5:p.Gly782Asp
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.406G>A
  hgvsp: ENSP00000334127.6:p.Gly136Asp
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2550G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1403G>A
  hgvsp: ENSP00000365872.4:p.Gly468Asp
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3416
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly782Asp
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-131620662-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620662
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620662
    reference: chr 12
allele count: 2
allele frequency: 1.660191918185742e-5
allele num: 120468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.905G>T
  hgvsp: ENSP00000438021.1:p.Cys302Phe
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2444G>T
  hgvsp: ENSP00000444425.1:p.Cys815Phe
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2348G>T
  hgvsp: ENSP00000261654.5:p.Cys783Phe
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1406G>T
  hgvsp: ENSP00000365872.4:p.Cys469Phe
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.409G>T
  hgvsp: ENSP00000334127.6:p.Cys137Phe
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.388G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2553G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.215G>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14506
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10536
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys783Phe
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

12-131620682-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620682
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620682
    reference: chr 12
allele count: 1
allele frequency: 8.333611120370679e-6
allele num: 119996
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.925A>G
  hgvsp: ENSP00000438021.1:p.Met309Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.429A>G
  hgvsp: ENSP00000334127.6:p.Met144Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2464A>G
  hgvsp: ENSP00000444425.1:p.Met822Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.235A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2573A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2368A>G
  hgvsp: ENSP00000261654.5:p.Met790Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1426A>G
  hgvsp: ENSP00000365872.4:p.Met476Val
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.408A>G
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10271
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met790Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

12-131620683-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620683
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620683
    reference: chr 12
allele count: 1
allele frequency: 8.33694600993764e-6
allele num: 119948
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.236T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2465T>C
  hgvsp: ENSP00000444425.1:p.Met822Thr
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2574T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.926T>C
  hgvsp: ENSP00000438021.1:p.Met309Thr
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2369T>C
  hgvsp: ENSP00000261654.5:p.Met790Thr
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.409T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1427T>C
  hgvsp: ENSP00000365872.4:p.Met476Thr
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.430T>C
  hgvsp: ENSP00000334127.6:p.Met144Thr
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14194
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3326
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Met790Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

12-131620685-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620685
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620685
    reference: chr 12
allele count: 2
allele frequency: 1.668864004272292e-5
allele num: 119842
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1429T>C
  hgvsp: ENSP00000365872.4:p.Phe477Leu
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.411T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.432T>C
  hgvsp: ENSP00000334127.6:p.Phe145Leu
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2467T>C
  hgvsp: ENSP00000444425.1:p.Phe823Leu
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.238T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2371T>C
  hgvsp: ENSP00000261654.5:p.Phe791Leu
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.928T>C
  hgvsp: ENSP00000438021.1:p.Phe310Leu
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2576T>C
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6250
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10208
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe791Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

12-131620688-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620688
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620688
    reference: chr 12
allele count: 1
allele frequency: 8.351428094204109e-6
allele num: 119740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.241G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2374G>T
  hgvsp: ENSP00000261654.5:p.Ala792Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1432G>T
  hgvsp: ENSP00000365872.4:p.Ala478Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2470G>T
  hgvsp: ENSP00000444425.1:p.Ala824Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.435G>T
  hgvsp: ENSP00000334127.6:p.Ala146Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.931G>T
  hgvsp: ENSP00000438021.1:p.Ala311Ser
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.414G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2579G>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala792Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

12-131620692-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620692
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620692
    reference: chr 12
allele count: 4
allele frequency: 3.34627225271048e-5
allele num: 119536
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.935C>T
  hgvsp: ENSP00000438021.1:p.Thr312Met
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1436C>T
  hgvsp: ENSP00000365872.4:p.Thr479Met
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2378C>T
  hgvsp: ENSP00000261654.5:p.Thr793Met
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.439C>T
  hgvsp: ENSP00000334127.6:p.Thr147Met
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.418C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2583C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2474C>T
  hgvsp: ENSP00000444425.1:p.Thr825Met
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.245C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4493
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3206
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr793Met
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

12-131620693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620693
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620693
    reference: chr 12
allele count: 3
allele frequency: 2.510586305588565e-5
allele num: 119494
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.419G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2379G>A
  hgvsp: ENST00000261654.5:c.2379G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1437G>A
  hgvsp: ENST00000376682.4:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2475G>A
  hgvsp: ENST00000535015.1:c.2475G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.246G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2584G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.440G>A
  hgvsp: ENST00000335486.6:c.440G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.936G>A
  hgvsp: ENST00000543617.1:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13771
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr793Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-131620699-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620699
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620699
    reference: chr 12
allele count: 1
allele frequency: 8.386588168201411e-6
allele num: 119238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1443C>A
  hgvsp: ENSP00000365872.4:p.Asn481Lys
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2481C>A
  hgvsp: ENSP00000444425.1:p.Asn827Lys
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.252C>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.425C>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.446C>A
  hgvsp: ENSP00000334127.6:p.Asn149Lys
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2385C>A
  hgvsp: ENSP00000261654.5:p.Asn795Lys
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.942C>A
  hgvsp: ENSP00000438021.1:p.Asn314Lys
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2590C>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3095
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3456
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn795Lys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

12-131620711-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620711
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620711
    reference: chr 12
allele count: 1
allele frequency: 8.466396870819716e-6
allele num: 118114
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+3G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+3G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+3G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+3G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+3G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+3G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+3G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+3G>C
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6201
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3168
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1759
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2600
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2394+3G>C
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

12-131620713-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620713
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620713
    reference: chr 12
allele count: 1
allele frequency: 8.4870911343846e-6
allele num: 117826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+5G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+5G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+5G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+5G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+5G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+5G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+5G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+5G>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2793
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6095
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 2.75e1
  variant carriers: 0
hgvs: c.2394+5G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ

12-131620717-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620717
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620717
    reference: chr 12
allele count: 16
allele frequency: 1.361447218393152e-4
allele num: 117522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+9C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+9C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+9C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+9C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+9C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+9C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+9C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+9C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11675
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15489
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

12-131620718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620718
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620718
    reference: chr 12
allele count: 93
allele frequency: 8.062558518569893e-4
allele num: 115348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+10G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+10G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+10G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+10G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+10G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+10G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+10G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+10G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11505
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9144
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8345
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13444
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3596
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7318
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

12-131620719-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620719
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620719
    reference: chr 12
allele count: 2
allele frequency: 1.731511782937683e-5
allele num: 115506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+11C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+11C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+11C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+11C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+11C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+11C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+11C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+11C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4407
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5616
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1908
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 2.75e1
  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: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

12-131620720-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620720
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620720
    reference: chr 12
allele count: 8
allele frequency: 6.904408464804778e-5
allele num: 115868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+12G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+12G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+12G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+12G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+12G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+12G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+12G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+12G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4464
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3620
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum

12-131620722-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620722
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620722
    reference: chr 12
allele count: 1
allele frequency: 8.615936035290874e-6
allele num: 116064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+14G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+14G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+14G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+14G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+14G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+14G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+14G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+14G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6116
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7882
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4438
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD

12-131620722-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620722
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620722
    reference: chr 12
allele count: 1
allele frequency: 8.615936035290874e-6
allele num: 116064
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+14G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+14G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+14G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+14G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+14G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+14G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+14G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+14G>C
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6116
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4438
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

12-131620727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620727
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620727
    reference: chr 12
allele count: 3
allele frequency: 2.625315037804536e-5
allele num: 114272
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+19G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+19G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+19G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+19G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+19G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+19G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+19G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+19G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10323
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9407
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3495
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10955
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6428
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2815
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

12-131620729-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620729
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620729
    reference: chr 12
allele count: 1
allele frequency: 8.790126929432861e-6
allele num: 113764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+21C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+21C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+21C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+21C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+21C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+21C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+21C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+21C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8651
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12809
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3568
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11152
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3846
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6427
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-131620730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620730
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620730
    reference: chr 12
allele count: 2
allele frequency: 1.754663016967591e-5
allele num: 113982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+22G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+22G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+22G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+22G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+22G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+22G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+22G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+22G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12908
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8899
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7707
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3729
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3941
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1839
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-131620737-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620737
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620737
    reference: chr 12
allele count: 1
allele frequency: 8.985856262243229e-6
allele num: 111286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+29C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+29C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+29C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+29C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+29C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+29C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+29C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+29C>G
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12066
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3274
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6916
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4891
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6723
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2627
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

12-131620737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620737
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620737
    reference: chr 12
allele count: 51
allele frequency: 4.582786693744047e-4
allele num: 111286
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+29C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8532
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9266
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12066
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6916
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3972
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6723
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

12-131620738-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620738
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620738
    reference: chr 12
allele count: 70153
allele frequency: 6.297735964235057e-1
allele num: 111394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+30A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+30A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+30A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+30A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+30A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+30A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+30A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+30A>G
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 7.5e0
  variant carriers: 1763
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 705
genotype depth: GenotypeDepth
  all individuals: 12331
  bin: 2.25e1
  variant carriers: 11301
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.75e1
  variant carriers: 240
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 3.75e1
  variant carriers: 1983
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.25e1
  variant carriers: 304
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 1.25e1
  variant carriers: 6256
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 368
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 5.25e1
  variant carriers: 906
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.25e1
  variant carriers: 1303
genotype depth: GenotypeDepth
  all individuals: 13419
  bin: 1.75e1
  variant carriers: 11345
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.5e0
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 6.25e1
  variant carriers: 487
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 3.25e1
  variant carriers: 3661
genotype depth: GenotypeDepth
  all individuals: 8169
  bin: 2.75e1
  variant carriers: 7157
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 879
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.75e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.25e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 4.75e1
  variant carriers: 1130
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 1.25e1
  variant carriers: 220
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 7.5e0
  variant carriers: 183
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 3.25e1
  variant carriers: 928
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 8.75e1
  variant carriers: 709
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 1177
genotype quality: GenotypeQuality
  all individuals: 2987
  bin: 2.25e1
  variant carriers: 585
genotype quality: GenotypeQuality
  all individuals: 2034
  bin: 4.75e1
  variant carriers: 1819
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 2.5e0
  variant carriers: 122
num of homozygotes: 22098
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

12-131620743-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620743
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620743
    reference: chr 12
allele count: 2
allele frequency: 1.88821752265861e-5
allele num: 105920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+35C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+35C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+35C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+35C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+35C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+35C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+35C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+35C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18219
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6270
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12645
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 880
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8923
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6237
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

12-131620744-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620744
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620744
    reference: chr 12
allele count: 90
allele frequency: 8.583854723027621e-4
allele num: 104848
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+36G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+36G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+36G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+36G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+36G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+36G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+36G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+36G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13778
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18305
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4032
  bin: 9.75e1
  variant carriers: 90
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

12-131620752-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131620752
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131620752
    reference: chr 12
allele count: 1
allele frequency: 9.617234083477592e-6
allele num: 103980
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2394+44T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2490+44T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.455+44T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1452+44T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.261+44T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.951+44T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.434+44T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2599+44T>C
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5345
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6906
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12277
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3180
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

12-131621468-AACTAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621468
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621463
    reference: chr 12
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-49_1453-45delACTAC
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-49_262-45delACTAC
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-49_2491-45delACTAC
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-49_435-45delACTAC
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-49_2395-45delACTAC
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-49_456-45delACTAC
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-49_952-45delACTAC
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-49_2600-45delACTAC
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7807
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1794
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: AACTAC
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

12-131621470-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621470
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621470
    reference: chr 12
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-48C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-48C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-48C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-48C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-48C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-48C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-48C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-48C>G
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7807
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4167
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3791
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3291
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37703
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-131621471-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621471
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621471
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-47T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-47T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-47T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-47T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-47T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-47T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-47T>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-47T>C
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3307
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3794
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

12-131621471-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621471
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621471
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-47T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-47T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-47T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-47T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-47T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-47T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-47T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-47T>G
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4246
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

12-131621473-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621473
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621473
    reference: chr 12
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-45C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-45C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-45C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-45C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-45C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-45C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-45C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-45C>G
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7807
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

12-131621473-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621473
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621473
    reference: chr 12
allele count: 6
allele frequency: 4.943642475776152e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-45C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-45C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-45C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-45C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-45C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-45C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-45C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-45C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8158
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7807
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3298
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
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: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

12-131621474-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621474
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621474
    reference: chr 12
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-44G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-44G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-44G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-44G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-44G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-44G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-44G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-44G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3309
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2988
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4174
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

12-131621493-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621493
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621493
    reference: chr 12
allele count: 18
allele frequency: 1.482970554795762e-4
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-25C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-25C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-25C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-25C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-25C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-25C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-25C>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-25C>G
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3014
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

12-131621493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621493
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621493
    reference: chr 12
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-25C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-25C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-25C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-25C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-25C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-25C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-25C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-25C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3328
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37709
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3786
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-131621496-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621496
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621496
    reference: chr 12
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-22C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-22C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-22C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-22C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-22C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-22C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-22C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-22C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3021
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

12-131621497-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621497
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621497
    reference: chr 12
allele count: 52
allele frequency: 4.283995979634542e-4
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-21G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-21G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-21G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-21G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-21G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-21G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-21G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-21G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 7808
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3785
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4519
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4180
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37712
  bin: 9.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

12-131621497-G-GTTTCTTCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621497
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621506
    reference: chr 12
allele count: 3
allele frequency: 2.471536142096851e-5
allele num: 121382
alternate allele: GTTTCTTCCC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

12-131621505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621505
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621505
    reference: chr 12
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-13C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-13C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-13C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-13C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-13C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-13C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-13C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-13C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3792
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4538
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/12-131621506-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621506
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621506
    reference: chr 12
allele count: 5
allele frequency: 4.119023297195769e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-12C>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-12C>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-12C>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-12C>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-12C>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-12C>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-12C>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-12C>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4181
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

12-131621516-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621516
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621516
    reference: chr 12
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1453-2A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2600-2A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2395-2A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.952-2A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2491-2A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.262-2A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.435-2A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.456-2A>G
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37688
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4552
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 8.75e1
  variant carriers: 0
hgvs: c.2395-2A>G
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

12-131621523-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621523
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621523
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2400G>T
  hgvsp: ENST00000261654.5:c.2400G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2496G>T
  hgvsp: ENST00000535015.1:c.2496G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.957G>T
  hgvsp: ENST00000543617.1:c.957G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.267G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1458G>T
  hgvsp: ENST00000376682.4:c.1458G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.461G>T
  hgvsp: ENST00000335486.6:c.461G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.440G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2605G>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4556
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4181
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu800Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

12-131621547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621547
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621547
    reference: chr 12
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2520C>T
  hgvsp: ENST00000535015.1:c.2520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.291C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2424C>T
  hgvsp: ENST00000261654.5:c.2424C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1482C>T
  hgvsp: ENST00000376682.4:c.1482C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2629C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.485C>T
  hgvsp: ENST00000335486.6:c.485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.981C>T
  hgvsp: ENST00000543617.1:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.464C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37686
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu808Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

12-131621555-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621555
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621555
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.299C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1490C>T
  hgvsp: ENSP00000365872.4:p.Ser497Leu
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.493C>T
  hgvsp: ENSP00000334127.6:p.Ser165Leu
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.472C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2528C>T
  hgvsp: ENSP00000444425.1:p.Ser843Leu
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.989C>T
  hgvsp: ENSP00000438021.1:p.Ser330Leu
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2637C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2432C>T
  hgvsp: ENSP00000261654.5:p.Ser811Leu
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4537
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1792
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser811Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

12-131621563-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621563
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621563
    reference: chr 12
allele count: 4
allele frequency: 3.295001482750667e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+4C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+4C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+4C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.480C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+4C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+4C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+4C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+4C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37686
  bin: 9.75e1
  variant carriers: 4
hgvs: c.2436+4C>T
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

12-131621564-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621564
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621564
    reference: chr 12
allele count: 6
allele frequency: 4.942583653228331e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+5G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+5G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+5G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+5G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+5G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.481G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+5G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+5G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: c.2436+5G>A
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

12-131621567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621567
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621567
    reference: chr 12
allele count: 6
allele frequency: 4.94274651948266e-5
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+8C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+8C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+8C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+8C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+8C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.484C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+8C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+8C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37679
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: c.2436+8C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

12-131621568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621568
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621568
    reference: chr 12
allele count: 9
allele frequency: 7.414241934952384e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+9G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+9G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+9G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+9G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+9G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.485G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+9G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+9G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3030
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4181
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

12-131621571-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621571
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621571
    reference: chr 12
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+12C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+12C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.488C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+12C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+12C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+12C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+12C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+12C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

12-131621580-G-GGCAGGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621580
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621586
    reference: chr 12
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: GGCAGGT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+32_993+37dupGTGCAG
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+32_2532+37dupGTGCAG
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+32_497+37dupGTGCAG
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+32_1494+37dupGTGCAG
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+32_303+37dupGTGCAG
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.508_513dupGTGCAG
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+32_2641+37dupGTGCAG
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+32_2436+37dupGTGCAG
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37671
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

12-131621581-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621581
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621581
    reference: chr 12
allele count: 5
allele frequency: 4.119498409873614e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+22G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+22G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+22G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+22G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+22G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+22G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.498G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+22G>T
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8827
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3319
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

12-131621585-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621585
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621585
    reference: chr 12
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+26G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+26G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+26G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+26G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+26G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.502G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+26G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+26G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

12-131621587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621587
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621587
    reference: chr 12
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.504G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+28G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+28G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+28G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+28G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+28G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+28G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+28G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37665
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4172
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

12-131621588-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621588
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621588
    reference: chr 12
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.505C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+29C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+29C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2958
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4428
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

12-131621591-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621591
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621591
    reference: chr 12
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+32G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+32G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+32G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+32G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+32G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.508G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+32G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+32G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4356
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

12-131621593-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621593
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621593
    reference: chr 12
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+34G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+34G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+34G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+34G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+34G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+34G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+34G>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.510G>T
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8813
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2945
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37659
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

12-131621607-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131621607
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131621607
    reference: chr 12
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000537489
  gene symbol: GPR133
  hgvsc: ENST00000537489.1:n.524C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2532+48C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.303+48C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2436+48C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.993+48C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1494+48C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.497+48C>T
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.2641+48C>T
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8795
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3293
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3760
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1716
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

12-131622631-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131622631
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131622631
    reference: chr 12
allele count: 2
allele frequency: 1.788972771834413e-5
allele num: 111796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.994-51G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2437-51G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2533-51G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1495-51G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.498-51G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.304-51G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.3084G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11206
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7993
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8194
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14853
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

12-131622635-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131622635
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131622635
    reference: chr 12
allele count: 1
allele frequency: 8.648873051841344e-6
allele num: 115622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2533-47G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2437-47G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1495-47G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.304-47G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.498-47G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.3088G>A
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.994-47G>A
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1199
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

12-131622635-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131622635
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131622635
    reference: chr 12
allele count: 53
allele frequency: 4.583902717475913e-4
allele num: 115622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.498-47G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1495-47G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2533-47G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.3088G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2437-47G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.994-47G>C
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.304-47G>C
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12830
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11123
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4624
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3330
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

12-131622636-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131622636
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131622636
    reference: chr 12
allele count: 87
allele frequency: 8.057196836392599e-4
allele num: 107978
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.3089T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.304-46T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1495-46T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2533-46T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2437-46T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.994-46T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.498-46T>G
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7444
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14742
  bin: 9.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 5428
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 9942
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3264
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4598
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

12-131622637-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131622637
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131622637
    reference: chr 12
allele count: 1
allele frequency: 8.735608085678845e-6
allele num: 114474
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.304-45T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1495-45T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2437-45T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.3090T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.498-45T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.994-45T>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2533-45T>G
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10628
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5837
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10816
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

12-131622640-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131622640
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 131622640
    reference: chr 12
allele count: 1
allele frequency: 8.630808534143478e-6
allele num: 115864
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000261654
  ensembl transcript: ENST00000261654
  gene symbol: GPR133
  hgvsc: ENST00000261654.5:c.2437-42A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000540207
  gene symbol: GPR133
  hgvsc: ENST00000540207.1:n.304-42A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000444425
  ensembl transcript: ENST00000535015
  gene symbol: GPR133
  hgvsc: ENST00000535015.1:c.2533-42A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111452
  ensembl transcript: ENST00000446583
  gene symbol: GPR133
  hgvsc: ENST00000446583.2:n.3093A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000334127
  ensembl transcript: ENST00000335486
  gene symbol: GPR133
  hgvsc: ENST00000335486.6:c.498-42A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000365872
  ensembl transcript: ENST00000376682
  gene symbol: GPR133
  hgvsc: ENST00000376682.4:c.1495-42A>G
  variant of: http://identifiers.org/hgnc/19893
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111452
  ensembl protein: ENSP00000438021
  ensembl transcript: ENST00000543617
  gene symbol: GPR133
  hgvsc: ENST00000543617.1:c.994-42A>G
  variant of: http://identifiers.org/hgnc/19893
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6021
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3803
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31266
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6500
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10625
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.0262e6

MQRankSum
type: SiteQuality
SIO_000300: -1.227e0

FS
type: SiteQuality
SIO_000300: 4.057e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.261e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: -1.359e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6519
bin: 9.75e1
variant carriers: 38

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1025
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3796
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10632
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31301
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.468007629616785e-4
allele num: 11534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.574803149606299e-4
allele num: 6350
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.669309611293754e-4
allele num: 10342
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 3.311158604497155e-4
allele num: 66442
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

DP
type: SiteQuality
SIO_000300: 2.026228e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.99e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6479
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.011503945070168e-5
allele num: 66412
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.337e1

FS
type: SiteQuality
SIO_000300: 6.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.605e0

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 2.023017e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.63e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-1

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

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10607
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6618
bin: 9.75e1
variant carriers: 381

European (Finnish)
type: Population
allele count: 23
allele frequency: 3.631196716135144e-3
allele num: 6334
num of homozygotes: 0

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

South Asian
type: Population
allele count: 60
allele frequency: 3.641218594489622e-3
allele num: 16478
num of homozygotes: 2

Latino
type: Population
allele count: 14
allele frequency: 1.214434420541291e-3
allele num: 11528
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.673050880247631e-4
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 278
allele frequency: 4.185738376294869e-3
allele num: 66416
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.88e-1

DP
type: SiteQuality
SIO_000300: 2.030278e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.256e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

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

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

GenotypeQuality
all individuals: 3436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6274
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3771
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506024096385542e-5
allele num: 66400
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.800000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.569e0

MQRankSum
type: SiteQuality
SIO_000300: -7.95e-1

DP
type: SiteQuality
SIO_000300: 2.014085e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.03e0

MQ
type: SiteQuality
SIO_000300: 5.892e1

VQSLOD
type: SiteQuality
SIO_000300: -1.311e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.42e-1

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3764
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6273
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2066
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10612
bin: 6.75e1
variant carriers: 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: 10336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.809e0

QD
type: SiteQuality
SIO_000300: 9.699999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.014093e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 1.501e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.334e0

VQSLOD
type: SiteQuality
SIO_000300: -1.106e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 3762
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6277
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2062
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 725
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10612
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31355
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.037777911670784e-5
allele num: 66388
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.076072426783327e-5
allele num: 16458
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.013179e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 1.787e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.320000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

QD
type: SiteQuality
SIO_000300: 1.266e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

GenotypeQuality
all individuals: 721
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31242
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 178
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2057
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 778
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10570
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.077549532028686e-5
allele num: 16454
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.936858415649816e-4
allele num: 10326
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.63284688441047e-4
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

DP
type: SiteQuality
SIO_000300: 2.011786e6

QD
type: SiteQuality
SIO_000300: 1.252e1

FS
type: SiteQuality
SIO_000300: 1.3569e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.68e0

MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQ
type: SiteQuality
SIO_000300: 5.895e1

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 719
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1001
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3742
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10556
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31196
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.0790273556231e-5
allele num: 16450
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66364
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.010551e6

VQSLOD
type: SiteQuality
SIO_000300: -4.764e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.109e0

FS
type: SiteQuality
SIO_000300: 2.156e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

GenotypeQuality
all individuals: 840
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31308
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6269
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014136299243452e-5
allele num: 66354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
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: 8632
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: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.56e-1

QD
type: SiteQuality
SIO_000300: 1.365e1

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 4.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.386e0

MQRankSum
type: SiteQuality
SIO_000300: -5.28e-1

DP
type: SiteQuality
SIO_000300: 2.009832e6

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30265
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6254
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6228
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

QD
type: SiteQuality
SIO_000300: 1.436e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

VQSLOD
type: SiteQuality
SIO_000300: 3.74e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

DP
type: SiteQuality
SIO_000300: 1.986717e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

GenotypeQuality
all individuals: 371
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30065
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6226
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.105006105006105e-5
allele num: 16380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66158
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.873e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.984334e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.51e-1

GenotypeQuality
all individuals: 3604
bin: 7.75e1
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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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
all individuals: 29516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.948558067030398e-4
allele num: 10264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.978213e6

MQRankSum
type: SiteQuality
SIO_000300: -2.53e-1

FS
type: SiteQuality
SIO_000300: 2.123e0

QD
type: SiteQuality
SIO_000300: 1.125e1

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 698
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66074
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.773469029654326e-5
allele num: 11398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 2.921e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

FS
type: SiteQuality
SIO_000300: 3.638e0

VQSLOD
type: SiteQuality
SIO_000300: -5.228e0

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.331e0

DP
type: SiteQuality
SIO_000300: 1.972606e6

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

GenotypeQuality
all individuals: 36
bin: 1.75e1
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: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.930259816370385e-4
allele num: 10238
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515472979116782e-5
allele num: 65986
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 1.958588e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 3.208e0

QD
type: SiteQuality
SIO_000300: 1.501e1

MQRankSum
type: SiteQuality
SIO_000300: 3.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

GenotypeQuality
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bin: 6.75e1
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: 3

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: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031864900100051e-5
allele num: 65966
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.80126738250308e-5
allele num: 11362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.199e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

DP
type: SiteQuality
SIO_000300: 1.957862e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.309e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

GenotypeQuality
all individuals: 9624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 27748
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variant carriers: 0

GenotypeQuality
all individuals: 1860
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51828009231143e-5
allele num: 65864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 1.551e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.222e0

VQSLOD
type: SiteQuality
SIO_000300: 5.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

DP
type: SiteQuality
SIO_000300: 1.935519e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

GenotypeQuality
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bin: 2.5e0
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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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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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
all individuals: 537
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6026
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530971554548516e-5
allele num: 65318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16236
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.289e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: 7.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.753e0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

QD
type: SiteQuality
SIO_000300: 1.004e1

DP
type: SiteQuality
SIO_000300: 1.856792e6

GenotypeQuality
all individuals: 6199
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1752
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65162
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.005763688760806e-5
allele num: 11104
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5996
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.232e0

DP
type: SiteQuality
SIO_000300: 1.83776e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.511e1

MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
all individuals: 3636
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
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GenotypeQuality
all individuals: 2671
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
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variant carriers: 0

GenotypeQuality
all individuals: 2742
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6203
bin: 9.75e1
variant carriers: 16

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.075976622577668e-5
allele num: 65020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11060
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.173601679219657e-5
allele num: 16198
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.0e-4
allele num: 10000
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.427891480247501e-3
allele num: 8404
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

DP
type: SiteQuality
SIO_000300: 1.812818e6

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

FS
type: SiteQuality
SIO_000300: 6.592e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.262e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
all individuals: 4501
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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variant carriers: 93

GenotypeQuality
all individuals: 791
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.182033096926714e-3
allele num: 846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 80
allele frequency: 1.25344697919278e-3
allele num: 63824
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.214267959234402e-5
allele num: 16092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5756
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.605747973470892e-4
allele num: 10856
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.188118811881188e-4
allele num: 9696
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.792e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.73e0

DP
type: SiteQuality
SIO_000300: 1.704315e6

QD
type: SiteQuality
SIO_000300: 1.314e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
all individuals: 4501
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563819472680074e-5
allele num: 63946
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.030927835051546e-4
allele num: 9700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10870
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16106
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

DP
type: SiteQuality
SIO_000300: 1.699805e6

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

QD
type: SiteQuality
SIO_000300: 8.289999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

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
all individuals: 1053
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10888
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.022704029453876e-4
allele num: 9778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.348906560636183e-4
allele num: 16096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64162
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

FS
type: SiteQuality
SIO_000300: 1.602e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.18e-2

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 3.323e1

DP
type: SiteQuality
SIO_000300: 1.694612e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.850000000000001e-1

GenotypeQuality
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bin: 8.25e1
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
all individuals: 16776
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GenotypeQuality
all individuals: 1327
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10896
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.206554121151936e-5
allele num: 16112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

DP
type: SiteQuality
SIO_000300: 1.691243e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.184e1

GenotypeQuality
all individuals: 790
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
all individuals: 16776
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variant carriers: 0

GenotypeQuality
all individuals: 524
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.177679882525697e-5
allele num: 10896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

DP
type: SiteQuality
SIO_000300: 1.691243e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

QD
type: SiteQuality
SIO_000300: 1.184e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
all individuals: 1018
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.215362177929023e-4
allele num: 8228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63250
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.247972045426183e-4
allele num: 16026
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.631277e6

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

FS
type: SiteQuality
SIO_000300: 1.556e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.765e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8206
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63002
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.252344629235963e-5
allele num: 15994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

QD
type: SiteQuality
SIO_000300: 1.666e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.021e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 1.624698e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-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: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10682
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63212
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 1
allele frequency: 1.042970379641218e-4
allele num: 9588
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Other
type: Population
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South Asian
type: Population
allele count: 1
allele frequency: 6.264094211976948e-5
allele num: 15964
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.354e0

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.61355e6

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61812
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10428
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.070663811563169e-4
allele num: 9340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5078
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15810
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

QD
type: SiteQuality
SIO_000300: 1.559e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

DP
type: SiteQuality
SIO_000300: 1.579432e6

GenotypeQuality
all individuals: 1486
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6550
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6086
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2627
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6151
bin: 9.75e1
variant carriers: 51

GenotypeQuality
all individuals: 3677
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4891
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.589566551591868e-5
allele num: 10428
num of homozygotes: 0

African
type: Population
allele count: 49
allele frequency: 5.246252676659529e-3
allele num: 9340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.325110689437066e-5
allele num: 15810
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

DP
type: SiteQuality
SIO_000300: 1.579432e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

QD
type: SiteQuality
SIO_000300: 1.559e1

GenotypeQuality
all individuals: 1103
bin: 4.25e1
variant carriers: 849

GenotypeQuality
all individuals: 2026
bin: 3.75e1
variant carriers: 1270

GenotypeQuality
all individuals: 1388
bin: 2.75e1
variant carriers: 478

GenotypeQuality
all individuals: 31227
bin: 9.75e1
variant carriers: 30750

GenotypeQuality
all individuals: 3410
bin: 6.25e1
variant carriers: 2154

GenotypeQuality
all individuals: 715
bin: 1.75e1
variant carriers: 450

GenotypeQuality
all individuals: 1624
bin: 7.75e1
variant carriers: 1505

GenotypeQuality
all individuals: 1128
bin: 7.25e1
variant carriers: 1025

GenotypeQuality
all individuals: 993
bin: 9.25e1
variant carriers: 938

GenotypeQuality
all individuals: 2254
bin: 6.75e1
variant carriers: 1976

GenotypeQuality
all individuals: 2103
bin: 5.25e1
variant carriers: 1967

GenotypeQuality
all individuals: 1473
bin: 8.25e1
variant carriers: 1390

Other
type: Population
allele count: 521
allele frequency: 6.369193154034229e-1
allele num: 818
num of homozygotes: 168

African
type: Population
allele count: 6455
allele frequency: 6.79903096692648e-1
allele num: 9494
num of homozygotes: 2158

East Asian
type: Population
allele count: 3656
allele frequency: 4.654952890247008e-1
allele num: 7854
num of homozygotes: 783

European (Non-Finnish)
type: Population
allele count: 42225
allele frequency: 6.811802284313093e-1
allele num: 61988
num of homozygotes: 14088

South Asian
type: Population
allele count: 10166
allele frequency: 6.405797101449275e-1
allele num: 15870
num of homozygotes: 3284

Latino
type: Population
allele count: 3934
allele frequency: 3.885815883050178e-1
allele num: 10124
num of homozygotes: 694

European (Finnish)
type: Population
allele count: 3196
allele frequency: 6.09226077011056e-1
allele num: 5246
num of homozygotes: 923

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.26e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

DP
type: SiteQuality
SIO_000300: 1.549423e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

QD
type: SiteQuality
SIO_000300: 2.577e1

VQSLOD
type: SiteQuality
SIO_000300: 3.95e0

GenotypeQuality
all individuals: 833
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3967
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 749
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
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variant carriers: 0

GenotypeQuality
all individuals: 1056
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variant carriers: 0

GenotypeQuality
all individuals: 5231
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variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 937
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variant carriers: 0

GenotypeQuality
all individuals: 2179
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variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.69664065151001e-5
allele num: 58940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.574621959237344e-5
allele num: 15210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4772
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.183e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

DP
type: SiteQuality
SIO_000300: 1.241243e6

VQSLOD
type: SiteQuality
SIO_000300: -1.536e0

QD
type: SiteQuality
SIO_000300: 1.647e1

MQ
type: SiteQuality
SIO_000300: 5.806e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

GenotypeQuality
all individuals: 1030
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8171
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12683
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2268
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
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variant carriers: 0

GenotypeQuality
all individuals: 606
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variant carriers: 0

GenotypeQuality
all individuals: 851
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variant carriers: 1

GenotypeQuality
all individuals: 5178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 877
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9165
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 3.116559318512362e-4
allele num: 9626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.427004797806717e-5
allele num: 58360
num of homozygotes: 0

South Asian
type: Population
allele count: 85
allele frequency: 5.622436830268554e-3
allele num: 15118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8874
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

DP
type: SiteQuality
SIO_000300: 1.238598e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.053e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

GenotypeQuality
all individuals: 8627
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1913
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
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variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6760
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3958
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8844
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.059322033898305e-4
allele num: 9440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15018
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQ
type: SiteQuality
SIO_000300: 5.907e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 1.210439e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.49e-1

QD
type: SiteQuality
SIO_000300: 1.75e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 3803
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 4037
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variant carriers: 0

GenotypeQuality
all individuals: 181
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variant carriers: 0

GenotypeQuality
all individuals: 2313
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variant carriers: 0

GenotypeQuality
all individuals: 37708
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3302
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 11570
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
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: 66714
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.484e0

DP
type: SiteQuality
SIO_000300: 3.078422e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 2.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.097e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.9e-1

FS
type: SiteQuality
SIO_000300: 1.653e0

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

MQ
type: SiteQuality
SIO_000300: 5.739e1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 1779
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variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4171
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 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: 10396
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
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: 8648
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: 66712
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.919e0

MQRankSum
type: SiteQuality
SIO_000300: 4.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

DP
type: SiteQuality
SIO_000300: 3.078709e6

QD
type: SiteQuality
SIO_000300: 1.562e1

MQ
type: SiteQuality
SIO_000300: 5.886e1

VQSLOD
type: SiteQuality
SIO_000300: -1.561e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.47e0

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

GenotypeQuality
all individuals: 4246
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variant carriers: 0

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

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 4173
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 2315
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37703
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 2988
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1789
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

QD
type: SiteQuality
SIO_000300: 9.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

VQSLOD
type: SiteQuality
SIO_000300: -4.083e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 3.078937e6

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeQuality
all individuals: 2315
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3307
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 3794
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1789
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 37703
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

InbreedingCoeff
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SIO_000300: 8.0e-4

MQRankSum
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BaseQRankSum
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SIO_000300: 2.92e0

MQ
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SIO_000300: 5.931e1

FS
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SIO_000300: 0.0e0

DP
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ClippingRankSum
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SIO_000300: 1.39e0

VQSLOD
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QD
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SIO_000300: 9.35e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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SIO_000300: 1.276e1

VQSLOD
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DP
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 7.75e-1

MQRankSum
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

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

ClippingRankSum
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SIO_000300: -7.17e-1

InbreedingCoeff
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MQRankSum
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QD
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MQ
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VQSLOD
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 7.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

DP
type: SiteQuality
SIO_000300: 3.079403e6

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: 0

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

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

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

African
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allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 3.079677e6

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-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: 0

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

European (Non-Finnish)
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allele count: 15
allele frequency: 2.248134048739546e-4
allele num: 66722
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
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.86e-1

FS
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

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: 0

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

African
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allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8652
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66722
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Other
type: Population
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allele num: 908
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South Asian
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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QD
type: SiteQuality
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 2.997422216893472e-5
allele num: 66724
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East Asian
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allele frequency: 0.0e0
allele num: 8652
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European (Finnish)
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num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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Latino
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allele frequency: 2.592464569650881e-4
allele num: 11572
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African
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allele frequency: 4.710632570659489e-3
allele num: 10402
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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Other
type: Population
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BaseQRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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Other
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European (Non-Finnish)
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African
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South Asian
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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MQ
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QD
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FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeQuality
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variant carriers: 0

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

East Asian
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South Asian
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Latino
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African
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European (Non-Finnish)
type: Population
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allele num: 66728
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Other
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European (Finnish)
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ClippingRankSum
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SIO_000300: 1.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.68e-1

FS
type: SiteQuality
SIO_000300: 8.445e0

QD
type: SiteQuality
SIO_000300: 4.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 3.080485e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: -1.965e0

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

GenotypeQuality
all individuals: 1784
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2324
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
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: 908
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 3.080623e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.432e0

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.098000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.36e-2

QD
type: SiteQuality
SIO_000300: 1.267e1

FS
type: SiteQuality
SIO_000300: 3.408e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3330
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
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: 908
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: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 6.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.08064e6

MQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e0

FS
type: SiteQuality
SIO_000300: 4.301e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.443e0

VQSLOD
type: SiteQuality
SIO_000300: -3.656e0

GenotypeQuality
all individuals: 2325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1786
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
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: 11574
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 3.080628e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.45e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.056e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.61e-1

QD
type: SiteQuality
SIO_000300: 1.024e1

GenotypeQuality
all individuals: 3026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 4550
bin: 6.25e1
variant carriers: 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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
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: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.335e0

DP
type: SiteQuality
SIO_000300: 3.080514e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.215e0

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.214e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.951e1

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3328
bin: 7.75e1
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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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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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
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: 10404
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: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
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: 8652
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.080396e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.52e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 7.849e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.905e0

MQRankSum
type: SiteQuality
SIO_000300: -2.66e-1

QD
type: SiteQuality
SIO_000300: 1.73e1

VQSLOD
type: SiteQuality
SIO_000300: -4.902e-1

GenotypeQuality
all individuals: 3326
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1789
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

DP
type: SiteQuality
SIO_000300: 3.080331e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.284e1

MQRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.24e-1

GenotypeQuality
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bin: 8.75e1
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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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.991727610598249e-5
allele num: 66728
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.227e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e-1

DP
type: SiteQuality
SIO_000300: 3.080112e6

QD
type: SiteQuality
SIO_000300: 1.236e1

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

GenotypeQuality
all individuals: 9
bin: 2.75e1
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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
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: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
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: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

FS
type: SiteQuality
SIO_000300: 2.178e0

QD
type: SiteQuality
SIO_000300: 1.174e1

DP
type: SiteQuality
SIO_000300: 3.080095e6

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 9

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.198932949674789e-4
allele num: 66726
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: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

African
type: Population
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.01e-1

BaseQRankSum
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SIO_000300: -2.487e0

DP
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FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
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SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.196e1

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

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: 0

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: -9.350000000000001e-1

InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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MQRankSum
type: SiteQuality
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FS
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MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
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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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
allele num: 8652
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.35e-1

FS
type: SiteQuality
SIO_000300: 4.482e0

MQ
type: SiteQuality
SIO_000300: 5.289e1

MQRankSum
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.404e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.078349e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-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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variant carriers: 0

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

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

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

Latino
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allele count: 5
allele frequency: 4.320774282751469e-4
allele num: 11572
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.236e0

FS
type: SiteQuality
SIO_000300: 6.915e0

DP
type: SiteQuality
SIO_000300: 3.077958e6

QD
type: SiteQuality
SIO_000300: 1.338e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-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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African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
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East Asian
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allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.519e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.077509e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.69e-1

FS
type: SiteQuality
SIO_000300: 1.3008e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.698e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.291e1

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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66710
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East Asian
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allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

Latino
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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: 908
num of homozygotes: 0

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

South Asian
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.741e0

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

DP
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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QD
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-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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Other
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allele num: 908
num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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Latino
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allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 2.311604253351826e-4
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FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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QD
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MQ
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66710
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Other
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African
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European (Finnish)
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Latino
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East Asian
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InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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ClippingRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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Other
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European (Finnish)
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African
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MQ
type: SiteQuality
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BaseQRankSum
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FS
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DP
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Latino
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Other
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African
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South Asian
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 1.4751e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.343e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 3.067143e6

QD
type: SiteQuality
SIO_000300: 9.49e0

VQSLOD
type: SiteQuality
SIO_000300: -2.842e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.42e-1

GenotypeQuality
all individuals: 1137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4588
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4191
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3149
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5528
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2317
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3318
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.191043353978085e-4
allele num: 8396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8884
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

FS
type: SiteQuality
SIO_000300: 1.376e0

DP
type: SiteQuality
SIO_000300: 1.951074e6

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.077e0

VQSLOD
type: SiteQuality
SIO_000300: -6.57e-1

QD
type: SiteQuality
SIO_000300: 1.729e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.5e-1

GenotypeQuality
all individuals: 2574
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5720
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14900
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 464
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4624
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.584133320660267e-5
allele num: 63126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

FS
type: SiteQuality
SIO_000300: 5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

QD
type: SiteQuality
SIO_000300: 1.448e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.84e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

DP
type: SiteQuality
SIO_000300: 1.929248e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.73e-1

GenotypeQuality
all individuals: 2336
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5720
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2574
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14900
bin: 9.75e1
variant carriers: 53

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.782715615668365e-5
allele num: 11386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63126
num of homozygotes: 0

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

African
type: Population
allele count: 52
allele frequency: 5.50381033022862e-3
allele num: 9448
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

DP
type: SiteQuality
SIO_000300: 1.929248e6

FS
type: SiteQuality
SIO_000300: 5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

QD
type: SiteQuality
SIO_000300: 1.448e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 2296
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 294
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 629
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 592
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 304
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1066
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1285
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 4506
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3103
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4091
bin: 8.25e1
variant carriers: 2

East Asian
type: Population
allele count: 1
allele frequency: 1.202790473899447e-4
allele num: 8314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.944012441679627e-4
allele num: 5144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 63
allele frequency: 1.087857438872773e-3
allele num: 57912
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.098304671301378e-5
allele num: 16398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

African
type: Population
allele count: 21
allele frequency: 2.557856272838002e-3
allele num: 8210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.261799999999999e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.162e0

VQSLOD
type: SiteQuality
SIO_000300: -3.269e1

MQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

QD
type: SiteQuality
SIO_000300: 2.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.191e0

DP
type: SiteQuality
SIO_000300: 1.857365e6

GenotypeQuality
all individuals: 4704
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4255
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15024
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 463
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3279
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3372
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1338
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62398
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.083658430862592e-4
allele num: 9228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5764
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.898e0

DP
type: SiteQuality
SIO_000300: 1.843455e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.77e-2

QD
type: SiteQuality
SIO_000300: 1.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.496e0

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.617e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e0