8-85785546-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785546
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785546
    reference: chr 8
allele count: 1
allele frequency: 2.188662727073758e-5
allele num: 45690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.599A>G
  hgvsp: ENSP00000430367.1:p.Lys200Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.599A>G
  hgvsp: ENSP00000430394.1:p.Lys200Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.332A>G
  hgvsp: ENSP00000428310.1:p.Lys111Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.566A>G
  hgvsp: ENSP00000430065.1:p.Lys189Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.830A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.380A>G
  hgvsp: ENSP00000428807.1:p.Lys127Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.599A>G
  hgvsp: ENSP00000428667.1:p.Lys200Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.638A>G
  hgvsp: ENSP00000430128.1:p.Lys213Arg
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12588
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys213Arg
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD

8-85785558-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785558
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785558
    reference: chr 8
allele count: 31
allele frequency: 6.105727566375167e-4
allele num: 50772
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.650C>G
  hgvsp: ENSP00000430128.1:p.Thr217Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.611C>G
  hgvsp: ENSP00000430367.1:p.Thr204Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.392C>G
  hgvsp: ENSP00000428807.1:p.Thr131Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.578C>G
  hgvsp: ENSP00000430065.1:p.Thr193Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.611C>G
  hgvsp: ENSP00000430394.1:p.Thr204Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.611C>G
  hgvsp: ENSP00000428667.1:p.Thr204Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.344C>G
  hgvsp: ENSP00000428310.1:p.Thr115Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.842C>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31994
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13926
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14860
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr217Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

8-85785562-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785562
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785562
    reference: chr 8
allele count: 61
allele frequency: 1.160710887848689e-3
allele num: 52554
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.846G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.348G>A
  hgvsp: ENST00000521376.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.582G>A
  hgvsp: ENST00000518566.1:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.615G>A
  hgvsp: ENST00000521268.1:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.654G>A
  hgvsp: ENST00000517638.1:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.615G>A
  hgvsp: ENST00000522455.1:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.615G>A
  hgvsp: ENST00000521695.1:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.396G>A
  hgvsp: ENST00000523850.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3840
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 31259
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14519
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15447
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln218Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

8-85785564-TCAAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785564
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785559
    reference: chr 8
allele count: 1
allele frequency: 1.882317509317472e-5
allele num: 53126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.619_623delAAAAC
  hgvsp: ENSP00000430367.1:p.Lys207Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.400_404delAAAAC
  hgvsp: ENSP00000428807.1:p.Lys134Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.352_356delAAAAC
  hgvsp: ENSP00000428310.1:p.Lys118Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.850_854delAAAAC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.619_623delAAAAC
  hgvsp: ENSP00000428667.1:p.Lys207Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.586_590delAAAAC
  hgvsp: ENSP00000430065.1:p.Lys196Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.619_623delAAAAC
  hgvsp: ENSP00000430394.1:p.Lys207Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.658_662delAAAAC
  hgvsp: ENSP00000430128.1:p.Lys220Ter
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15700
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31846
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys220Ter
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: TCAAAA
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ

8-85785576-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785576
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785576
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 54220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.860T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.410T>C
  hgvsp: ENSP00000428807.1:p.Ile137Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.629T>C
  hgvsp: ENSP00000430367.1:p.Ile210Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.629T>C
  hgvsp: ENSP00000428667.1:p.Ile210Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.629T>C
  hgvsp: ENSP00000430394.1:p.Ile210Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.596T>C
  hgvsp: ENSP00000430065.1:p.Ile199Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.362T>C
  hgvsp: ENSP00000428310.1:p.Ile121Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.668T>C
  hgvsp: ENSP00000430128.1:p.Ile223Thr
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30456
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14643
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile223Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

8-85785584-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785584
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785584
    reference: chr 8
allele count: 5
allele frequency: 9.149465671204801e-5
allele num: 54648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.370T>A
  hgvsp: ENSP00000428310.1:p.Leu124Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.637T>A
  hgvsp: ENSP00000430394.1:p.Leu213Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.676T>A
  hgvsp: ENSP00000430128.1:p.Leu226Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.868T>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.604T>A
  hgvsp: ENSP00000430065.1:p.Leu202Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.418T>A
  hgvsp: ENSP00000428807.1:p.Leu140Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.637T>A
  hgvsp: ENSP00000430367.1:p.Leu213Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.637T>A
  hgvsp: ENSP00000428667.1:p.Leu213Met
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30105
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2753
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14698
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31660
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu226Met
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

8-85785587-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785587
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785587
    reference: chr 8
allele count: 1
allele frequency: 1.835266480692997e-5
allele num: 54488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.640C>G
  hgvsp: ENSP00000430367.1:p.Leu214Val
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.607C>G
  hgvsp: ENSP00000430065.1:p.Leu203Val
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.679C>G
  hgvsp: ENSP00000430128.1:p.Leu227Val
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.373C>G
  hgvsp: ENSP00000428310.1:p.Leu125Val
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.421C>G
  hgvsp: ENSP00000428807.1:p.Leu141Val
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.640C>G
  hgvsp: ENSP00000428667.1:p.Leu214Val
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.871C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.640C>G
  hgvsp: ENSP00000430394.1:p.Leu214Val
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29964
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2937
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu227Val
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

8-85785590-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785590
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785590
    reference: chr 8
allele count: 1
allele frequency: 1.832777390858107e-5
allele num: 54562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.643G>A
  hgvsp: ENSP00000430394.1:p.Gly215Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.874G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.643G>A
  hgvsp: ENSP00000428667.1:p.Gly215Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.643G>A
  hgvsp: ENSP00000430367.1:p.Gly215Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.376G>A
  hgvsp: ENSP00000428310.1:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.610G>A
  hgvsp: ENSP00000430065.1:p.Gly204Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.424G>A
  hgvsp: ENSP00000428807.1:p.Gly142Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.682G>A
  hgvsp: ENSP00000430128.1:p.Gly228Arg
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13221
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly228Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

8-85785593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785593
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785593
    reference: chr 8
allele count: 1
allele frequency: 1.842774481258984e-5
allele num: 54266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.877C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.613C>T
  hgvsp: ENSP00000430065.1:p.Arg205Cys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.646C>T
  hgvsp: ENSP00000430394.1:p.Arg216Cys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.646C>T
  hgvsp: ENSP00000428667.1:p.Arg216Cys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.646C>T
  hgvsp: ENSP00000430367.1:p.Arg216Cys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.685C>T
  hgvsp: ENSP00000430128.1:p.Arg229Cys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.379C>T
  hgvsp: ENSP00000428310.1:p.Arg127Cys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.427C>T
  hgvsp: ENSP00000428807.1:p.Arg143Cys
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29727
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3196
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31941
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg229Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

8-85785594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785594
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785594
    reference: chr 8
allele count: 4
allele frequency: 7.400828892835997e-5
allele num: 54048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.380G>A
  hgvsp: ENSP00000428310.1:p.Arg127His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.647G>A
  hgvsp: ENSP00000430367.1:p.Arg216His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.878G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.614G>A
  hgvsp: ENSP00000430065.1:p.Arg205His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.686G>A
  hgvsp: ENSP00000430128.1:p.Arg229His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.428G>A
  hgvsp: ENSP00000428807.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.647G>A
  hgvsp: ENSP00000430394.1:p.Arg216His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.647G>A
  hgvsp: ENSP00000428667.1:p.Arg216His
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29696
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg229His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

8-85785594-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785594
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785594
    reference: chr 8
allele count: 2
allele frequency: 3.700414446417999e-5
allele num: 54048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.428G>T
  hgvsp: ENSP00000428807.1:p.Arg143Leu
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.614G>T
  hgvsp: ENSP00000430065.1:p.Arg205Leu
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.686G>T
  hgvsp: ENSP00000430128.1:p.Arg229Leu
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.878G>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.647G>T
  hgvsp: ENSP00000430394.1:p.Arg216Leu
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.647G>T
  hgvsp: ENSP00000430367.1:p.Arg216Leu
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.647G>T
  hgvsp: ENSP00000428667.1:p.Arg216Leu
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.380G>T
  hgvsp: ENSP00000428310.1:p.Arg127Leu
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12504
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13542
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg229Leu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-85785596-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785596
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785596
    reference: chr 8
allele count: 1
allele frequency: 1.842842400117942e-5
allele num: 54264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.430C>A
  hgvsp: ENSP00000428807.1:p.Leu144Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.649C>A
  hgvsp: ENSP00000428667.1:p.Leu217Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.649C>A
  hgvsp: ENSP00000430394.1:p.Leu217Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.616C>A
  hgvsp: ENSP00000430065.1:p.Leu206Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.688C>A
  hgvsp: ENSP00000430128.1:p.Leu230Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.880C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.649C>A
  hgvsp: ENSP00000430367.1:p.Leu217Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.382C>A
  hgvsp: ENSP00000428310.1:p.Leu128Met
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29725
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13861
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3343
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu230Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

8-85785606-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785606
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785606
    reference: chr 8
allele count: 1
allele frequency: 1.869787966044651e-5
allele num: 53482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.659T>C
  hgvsp: ENSP00000428667.1:p.Ile220Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.659T>C
  hgvsp: ENSP00000430367.1:p.Ile220Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.440T>C
  hgvsp: ENSP00000428807.1:p.Ile147Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.626T>C
  hgvsp: ENSP00000430065.1:p.Ile209Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.392T>C
  hgvsp: ENSP00000428310.1:p.Ile131Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.659T>C
  hgvsp: ENSP00000430394.1:p.Ile220Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.698T>C
  hgvsp: ENSP00000430128.1:p.Ile233Thr
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.890T>C
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile233Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-85785609-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785609
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785609
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 52326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.629A>C
  hgvsp: ENSP00000430065.1:p.Glu210Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.893A>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.701A>C
  hgvsp: ENSP00000430128.1:p.Glu234Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.662A>C
  hgvsp: ENSP00000430367.1:p.Glu221Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.662A>C
  hgvsp: ENSP00000430394.1:p.Glu221Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.443A>C
  hgvsp: ENSP00000428807.1:p.Glu148Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.395A>C
  hgvsp: ENSP00000428310.1:p.Glu132Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.662A>C
  hgvsp: ENSP00000428667.1:p.Glu221Ala
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29186
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4771
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32472
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu234Ala
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/8-85785617-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785617
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785617
    reference: chr 8
allele count: 93
allele frequency: 1.818679599499374e-3
allele num: 51136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.670C>A
  hgvsp: ENSP00000428667.1:p.Gln224Lys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.403C>A
  hgvsp: ENSP00000428310.1:p.Gln135Lys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.637C>A
  hgvsp: ENSP00000430065.1:p.Gln213Lys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.901C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.451C>A
  hgvsp: ENSP00000428807.1:p.Gln151Lys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.709C>A
  hgvsp: ENSP00000430128.1:p.Gln237Lys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.670C>A
  hgvsp: ENSP00000430367.1:p.Gln224Lys
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.670C>A
  hgvsp: ENSP00000430394.1:p.Gln224Lys
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28664
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8985
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8593
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5820
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10569
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln237Lys
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-85785619-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785619
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785619
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 50676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.453G>A
  hgvsp: ENST00000523850.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.639G>A
  hgvsp: ENST00000518566.1:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.405G>A
  hgvsp: ENST00000521376.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.672G>A
  hgvsp: ENST00000521268.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.672G>A
  hgvsp: ENST00000521695.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.711G>A
  hgvsp: ENST00000517638.1:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.672G>A
  hgvsp: ENST00000522455.1:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.903G>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28480
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32237
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln237Gln
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: QD

8-85785625-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785625
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785625
    reference: chr 8
allele count: 2
allele frequency: 4.073983541106494e-5
allele num: 49092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.645G>A
  hgvsp: ENST00000518566.1:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.411G>A
  hgvsp: ENST00000521376.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.717G>A
  hgvsp: ENST00000517638.1:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.678G>A
  hgvsp: ENST00000521695.1:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.678G>A
  hgvsp: ENST00000522455.1:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.678G>A
  hgvsp: ENST00000521268.1:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.459G>A
  hgvsp: ENST00000523850.1:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.909G>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7607
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1177
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala239Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

8-85785629-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785629
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785629
    reference: chr 8
allele count: 1
allele frequency: 2.091087783865167e-5
allele num: 47822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.415G>T
  hgvsp: ENSP00000428310.1:p.Ala139Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.463G>T
  hgvsp: ENSP00000428807.1:p.Ala155Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.682G>T
  hgvsp: ENSP00000430394.1:p.Ala228Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.682G>T
  hgvsp: ENSP00000430367.1:p.Ala228Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.721G>T
  hgvsp: ENSP00000430128.1:p.Ala241Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.649G>T
  hgvsp: ENSP00000430065.1:p.Ala217Ser
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.913G>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.682G>T
  hgvsp: ENSP00000428667.1:p.Ala228Ser
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1465
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9083
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8421
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala241Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-85785642-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785642
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785642
    reference: chr 8
allele count: 1
allele frequency: 2.267059623668102e-5
allele num: 44110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.652+10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.724+10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.685+10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.685+10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.685+10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.466+10C>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9465
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13045
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27013
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

8-85785642-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785642
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785642
    reference: chr 8
allele count: 3
allele frequency: 6.801178871004307e-5
allele num: 44110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.685+10C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+10C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+10C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.652+10C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.724+10C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.466+10C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.685+10C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.685+10C>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24725
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9465
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13045
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1601
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-85785653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785653
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785653
    reference: chr 8
allele count: 1
allele frequency: 2.540650406504065e-5
allele num: 39360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.685+21G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+21G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+21G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.652+21G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.685+21G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.466+21G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.685+21G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.724+21G>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1609
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2429
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3317
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

8-85785657-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785657
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785657
    reference: chr 8
allele count: 1
allele frequency: 2.657877950244525e-5
allele num: 37624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+25G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+25G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.652+25G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.724+25G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.685+25G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.685+25G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.685+25G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.466+25G>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7983
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18902
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18930
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1621
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2867
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

8-85785660-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785660
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785660
    reference: chr 8
allele count: 1
allele frequency: 2.7467999780256e-5
allele num: 36406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.685+28C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+28C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.724+28C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.685+28C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+28C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.652+28C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.685+28C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.466+28C>T
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4458
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19445
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3003
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4092
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1619
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17194
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-85785665-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785665
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785665
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 35400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.685+33T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+33T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.466+33T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.685+33T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.652+33T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.724+33T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.685+33T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+33T>C
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20981
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3648
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20234
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1679
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD

8-85785679-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785679
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785679
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 30988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.685+47C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.685+47C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+47C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.685+47C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.724+47C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.652+47C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+47C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.466+47C>T
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 20868
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21819
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2427
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18866
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

8-85785680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785680
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785680
    reference: chr 8
allele count: 1
allele frequency: 3.217089177712006e-5
allele num: 31084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.466+48G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.685+48G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+48G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.685+48G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.724+48G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.652+48G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.685+48G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+48G>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20876
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1897
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3622
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7111
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7418
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-85785681-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85785681
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85785681
    reference: chr 8
allele count: 2
allele frequency: 6.445375443119562e-5
allele num: 31030
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.466+49T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.685+49T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.685+49T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+49T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+49T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.685+49T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.652+49T>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.724+49T>C
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20891
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7807
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7115
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

8-85799798-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799798
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799798
    reference: chr 8
allele count: 1
allele frequency: 8.79786036036036e-6
allele num: 113664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-41G>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-41G>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-41G>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14166G>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-41G>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14166G>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-41G>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-41G>C
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3189
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5195
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/8-85799802-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799802
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799802
    reference: chr 8
allele count: 1
allele frequency: 8.790436005625879e-6
allele num: 113760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-37C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-37C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-37C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14170C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-37C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14170C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-37C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-37C>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3482
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1699
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11805
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23852
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

8-85799808-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799808
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799808
    reference: chr 8
allele count: 2
allele frequency: 1.756358016017985e-5
allele num: 113872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-31G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-31G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-31G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-31G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-31G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14176G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-31G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14176G>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23853
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

8-85799813-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799813
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799813
    reference: chr 8
allele count: 1
allele frequency: 8.807934187115753e-6
allele num: 113534
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-26A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14181A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-26A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-26A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-26A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-26A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-26A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14181A>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2626
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2814
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4340
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

8-85799824-TTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799824
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799822
    reference: chr 8
allele count: 1
allele frequency: 9.798926037706268e-6
allele num: 102052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-12_653-11delTC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-12_725-11delTC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-12_686-11delTC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14195_418+14196delTC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-12_686-11delTC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-12_686-11delTC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-12_467-11delTC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14195_916+14196delTC
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1043
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4431
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4385
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: TTC
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

8-85799827-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799827
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799827
    reference: chr 8
allele count: 1
allele frequency: 8.720676724513823e-6
allele num: 114670
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45991
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 13136
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11298
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8558
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9726
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

8-85799827-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799827
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799828
    reference: chr 8
allele count: 2483
allele frequency: 2.165344030696782e-2
allele num: 114670
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-3dupC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-3dupC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14204dupC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-3dupC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-3dupC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14204dupC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-3dupC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-3dupC
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 6.75e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 6.25e1
  variant carriers: 193
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 9.75e1
  variant carriers: 484
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 7.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.75e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 7.25e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 8.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 5.25e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 1.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 4.25e1
  variant carriers: 164
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 8.25e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 5.75e1
  variant carriers: 205
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 3.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 4.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 45991
  bin: 9.75e1
  variant carriers: 2373
num of homozygotes: 29
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS

8-85799827-T-TCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799827
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799829
    reference: chr 8
allele count: 12
allele frequency: 1.046481206941659e-4
allele num: 114670
alternate allele: TCC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-4_725-3dupCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-4_686-3dupCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-4_653-3dupCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14203_418+14204dupCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-4_467-3dupCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-4_686-3dupCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-4_686-3dupCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14203_916+14204dupCC
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 7.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

8-85799827-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799827
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799826
    reference: chr 8
allele count: 45509
allele frequency: 3.968692770558995e-1
allele num: 114670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-3delC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-3delC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-3delC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-3delC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-3delC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14204delC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-3delC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14204delC
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 600
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 7.75e1
  variant carriers: 2048
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.25e1
  variant carriers: 971
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 975
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 2.75e1
  variant carriers: 406
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 8.75e1
  variant carriers: 1539
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 620
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 321
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 5.75e1
  variant carriers: 2865
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 4.25e1
  variant carriers: 1560
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 6.75e1
  variant carriers: 2749
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 1.75e1
  variant carriers: 1158
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 6.25e1
  variant carriers: 2741
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.75e1
  variant carriers: 2096
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 5.25e1
  variant carriers: 2515
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 7.25e1
  variant carriers: 2394
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 9.75e1
  variant carriers: 7328
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 8.25e1
  variant carriers: 1761
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.25e1
  variant carriers: 1291
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 3.75e1
  variant carriers: 88
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.25e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 4.75e1
  variant carriers: 135
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 5.75e1
  variant carriers: 154
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 5.25e1
  variant carriers: 107
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 7.75e1
  variant carriers: 117
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 2.25e1
  variant carriers: 75
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 7.25e1
  variant carriers: 109
num of homozygotes: 10010
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: TC
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

8-85799827-TCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799827
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799825
    reference: chr 8
allele count: 20
allele frequency: 1.744135344902764e-4
allele num: 114670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-4_686-3delCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-4_467-3delCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14203_418+14204delCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-4_653-3delCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-4_725-3delCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-4_686-3delCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-4_686-3delCC
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14203_916+14204delCC
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: TCC
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-85799828-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799828
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799828
    reference: chr 8
allele count: 1
allele frequency: 2.505637684790779e-5
allele num: 39910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14196C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-11C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-11C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-11C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-11C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-11C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-11C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14196C>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-85799829-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799829
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799829
    reference: chr 8
allele count: 8
allele frequency: 1.771322292091046e-4
allele num: 45164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14197C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14197C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-10C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-10C>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19362
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12462
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

8-85799829-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799829
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799829
    reference: chr 8
allele count: 1
allele frequency: 2.214152865113807e-5
allele num: 45164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-10C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-10C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14197C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-10C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-10C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-10C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14197C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-10C>T
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19362
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-85799830-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799830
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799830
    reference: chr 8
allele count: 12
allele frequency: 1.014627547137905e-4
allele num: 118270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14198C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-9C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-9C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-9C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-9C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14198C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-9C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-9C>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

8-85799830-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799830
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799830
    reference: chr 8
allele count: 7
allele frequency: 5.918660691637778e-5
allele num: 118270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-9C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-9C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-9C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14198C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-9C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-9C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-9C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14198C>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

8-85799830-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799830
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799830
    reference: chr 8
allele count: 2
allele frequency: 1.691045911896508e-5
allele num: 118270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-9C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-9C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-9C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-9C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-9C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-9C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14198C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14198C>T
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

8-85799831-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799831
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799831
    reference: chr 8
allele count: 1
allele frequency: 8.43113449345744e-6
allele num: 118608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14199C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-8C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-8C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-8C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-8C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-8C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-8C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14199C>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2410
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
hgvs: c.725-8C>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-85799832-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799832
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799832
    reference: chr 8
allele count: 18
allele frequency: 1.517041432087112e-4
allele num: 118652
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-7C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-7C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-7C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14200C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-7C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14200C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-7C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-7C>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 2.75e1
  variant carriers: 0
hgvs: c.725-7C>A
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

8-85799832-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799832
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799832
    reference: chr 8
allele count: 6
allele frequency: 5.056804773623706e-5
allele num: 118652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-7C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-7C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-7C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14200C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-7C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-7C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-7C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14200C>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
hgvs: c.725-7C>G
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

8-85799832-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799832
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799832
    reference: chr 8
allele count: 4
allele frequency: 3.371203182415804e-5
allele num: 118652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14200C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-7C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-7C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-7C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-7C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-7C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-7C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14200C>T
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2703
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2417
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 7.25e1
  variant carriers: 0
hgvs: c.725-7C>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/8-85799833-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799833
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799833
    reference: chr 8
allele count: 7
allele frequency: 5.896723106730688e-5
allele num: 118710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14201C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-6C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-6C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-6C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14201C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-6C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-6C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-6C>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 38949
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
hgvs: c.725-6C>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/8-85799833-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799833
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799834
    reference: chr 8
allele count: 3
allele frequency: 2.527167045741723e-5
allele num: 118710
alternate allele: CA
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-6_725-5insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-6_653-5insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14201_418+14202insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-6_686-5insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-6_686-5insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-6_686-5insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-6_467-5insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14201_916+14202insA
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2707
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3809
  bin: 6.25e1
  variant carriers: 0
hgvs: c.725-6_725-5insA
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

8-85799833-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799833
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799833
    reference: chr 8
allele count: 17
allele frequency: 1.43206132592031e-4
allele num: 118710
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-6C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-6C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14201C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-6C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-6C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-6C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-6C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14201C>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2422
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
hgvs: c.725-6C>G
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-85799833-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799833
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799833
    reference: chr 8
allele count: 14
allele frequency: 1.179344621346138e-4
allele num: 118710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-6C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-6C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-6C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14201C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-6C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14201C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-6C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-6C>T
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2422
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
hgvs: c.725-6C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/8-85799834-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799834
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799834
    reference: chr 8
allele count: 63
allele frequency: 5.303833914229428e-4
allele num: 118782
alternate allele: A
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39016
  bin: 9.75e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2701
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6614
  num of homozygotes: 0
population: African
  type: Population
  allele count: 5
  allele frequency: 5.111429155591903e-4
  allele num: 9782
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 2
  allele frequency: 1.736714136853074e-4
  allele num: 11516
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 18
  allele frequency: 2.718540445840633e-4
  allele num: 66212
  num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-85799834-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799834
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799835
    reference: chr 8
allele count: 3
allele frequency: 2.525635197252109e-5
allele num: 118782
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-5_467-4insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14202_916+14203insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-5_686-4insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-5_725-4insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-5_686-4insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-5_686-4insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-5_653-4insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14202_418+14203insA
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
hgvs: c.725-5_725-4insA
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

8-85799834-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799834
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799835
    reference: chr 8
allele count: 1
allele frequency: 8.418783990840363e-6
allele num: 118782
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-5_686-4insT
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-5_686-4insT
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-5_725-4insT
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14202_916+14203insT
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-5_467-4insT
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-5_653-4insT
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-5_686-4insT
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14202_418+14203insT
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39016
  bin: 9.75e1
  variant carriers: 1
hgvs: c.725-5_725-4insT
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

8-85799834-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799834
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799834
    reference: chr 8
allele count: 91
allele frequency: 7.661093431664731e-4
allele num: 118782
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-5C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14202C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-5C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14202C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-5C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-5C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-5C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-5C>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 39016
  bin: 9.75e1
  variant carriers: 91
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
hgvs: c.725-5C>G
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

8-85799834-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799834
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799834
    reference: chr 8
allele count: 96
allele frequency: 8.082032631206748e-4
allele num: 118782
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2701
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39016
  bin: 9.75e1
  variant carriers: 95
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3867
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
  type: Population
  allele count: 17
  allele frequency: 1.476207016325113e-3
  allele num: 11516
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 4
  allele frequency: 2.636435539151068e-4
  allele num: 15172
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6614
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 888
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-85799835-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799835
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799835
    reference: chr 8
allele count: 34
allele frequency: 2.861808326178812e-4
allele num: 118806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-4C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14203C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-4C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-4C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14203C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-4C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-4C>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-4C>A
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2411
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
hgvs: c.725-4C>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/8-85799835-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799835
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799836
    reference: chr 8
allele count: 1
allele frequency: 8.417083312290625e-6
allele num: 118806
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14203_916+14204insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-4_467-3insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-4_653-3insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-4_686-3insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-4_686-3insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-4_725-3insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14203_418+14204insA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-4_686-3insA
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1666
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38952
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
hgvs: c.725-4_725-3insA
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

8-85799835-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799835
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799835
    reference: chr 8
allele count: 11
allele frequency: 9.258791643519688e-5
allele num: 118806
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-4C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-4C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-4C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14203C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14203C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-4C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-4C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-4C>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 7.25e1
  variant carriers: 0
hgvs: c.725-4C>G
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

8-85799835-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799835
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799835
    reference: chr 8
allele count: 2
allele frequency: 1.683416662458125e-5
allele num: 118806
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-4C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-4C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-4C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-4C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14203C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-4C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14203C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-4C>T
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38952
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1666
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
hgvs: c.725-4C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/8-85799836-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799836
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799837
    reference: chr 8
allele count: 1
allele frequency: 8.415808254224735e-6
allele num: 118824
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14205dupA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-2dupA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14205dupA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-2dupA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-2dupA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-2dupA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-2dupA
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-2dupA
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
hgvs: c.725-2dupA
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

8-85799836-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799836
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799836
    reference: chr 8
allele count: 1
allele frequency: 8.415808254224735e-6
allele num: 118824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.686-3C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.653-3C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14204C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.725-3C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.467-3C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.686-3C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.686-3C>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14204C>T
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38926
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
hgvs: c.725-3C>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

8-85799845-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799845
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799845
    reference: chr 8
allele count: 2
allele frequency: 1.676811375488371e-5
allele num: 119274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.659A>G
  hgvsp: ENSP00000430065.1:p.Gln220Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.692A>G
  hgvsp: ENSP00000428667.1:p.Gln231Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.692A>G
  hgvsp: ENSP00000430367.1:p.Gln231Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.473A>G
  hgvsp: ENSP00000428807.1:p.Gln158Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14213A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.692A>G
  hgvsp: ENSP00000430394.1:p.Gln231Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.731A>G
  hgvsp: ENSP00000430128.1:p.Gln244Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14213A>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2718
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln244Arg
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

8-85799846-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799846
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799846
    reference: chr 8
allele count: 1
allele frequency: 8.381667616588997e-6
allele num: 119308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14214G>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.693G>T
  hgvsp: ENSP00000430394.1:p.Gln231His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.660G>T
  hgvsp: ENSP00000430065.1:p.Gln220His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.693G>T
  hgvsp: ENSP00000430367.1:p.Gln231His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14214G>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.732G>T
  hgvsp: ENSP00000430128.1:p.Gln244His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.693G>T
  hgvsp: ENSP00000428667.1:p.Gln231His
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.474G>T
  hgvsp: ENSP00000428807.1:p.Gln158His
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln244His
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

8-85799854-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799854
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799854
    reference: chr 8
allele count: 1
allele frequency: 8.361204013377926e-6
allele num: 119600
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.701A>G
  hgvsp: ENSP00000428667.1:p.Gln234Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.701A>G
  hgvsp: ENSP00000430394.1:p.Gln234Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.668A>G
  hgvsp: ENSP00000430065.1:p.Gln223Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.701A>G
  hgvsp: ENSP00000430367.1:p.Gln234Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.740A>G
  hgvsp: ENSP00000430128.1:p.Gln247Arg
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14222A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14222A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.482A>G
  hgvsp: ENSP00000428807.1:p.Gln161Arg
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6035
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1609
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln247Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-85799865-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799865
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799865
    reference: chr 8
allele count: 3
allele frequency: 2.50141746989961e-5
allele num: 119932
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.751A>G
  hgvsp: ENSP00000430128.1:p.Ser251Gly
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14233A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.493A>G
  hgvsp: ENSP00000428807.1:p.Ser165Gly
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.712A>G
  hgvsp: ENSP00000430394.1:p.Ser238Gly
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.712A>G
  hgvsp: ENSP00000428667.1:p.Ser238Gly
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14233A>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.712A>G
  hgvsp: ENSP00000430367.1:p.Ser238Gly
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.679A>G
  hgvsp: ENSP00000430065.1:p.Ser227Gly
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2394
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser251Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

8-85799871-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799871
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799871
    reference: chr 8
allele count: 1
allele frequency: 8.322237017310253e-6
allele num: 120160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.499G>A
  hgvsp: ENSP00000428807.1:p.Val167Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.718G>A
  hgvsp: ENSP00000428667.1:p.Val240Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.718G>A
  hgvsp: ENSP00000430394.1:p.Val240Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.685G>A
  hgvsp: ENSP00000430065.1:p.Val229Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14239G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14239G>A
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.718G>A
  hgvsp: ENSP00000430367.1:p.Val240Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.757G>A
  hgvsp: ENSP00000430128.1:p.Val253Met
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38888
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7132
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val253Met
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

8-85799879-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799879
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799879
    reference: chr 8
allele count: 4
allele frequency: 3.323749854585944e-5
allele num: 120346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14247C>G
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.693C>G
  hgvsp: ENSP00000430065.1:p.Ile231Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.765C>G
  hgvsp: ENSP00000430128.1:p.Ile255Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.726C>G
  hgvsp: ENSP00000430367.1:p.Ile242Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.726C>G
  hgvsp: ENSP00000428667.1:p.Ile242Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.726C>G
  hgvsp: ENSP00000430394.1:p.Ile242Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.507C>G
  hgvsp: ENSP00000428807.1:p.Ile169Met
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14247C>G
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5908
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7448
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2652
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2450
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38887
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile255Met
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

8-85799883-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799883
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799883
    reference: chr 8
allele count: 1
allele frequency: 8.301510874979247e-6
allele num: 120460
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.697G>T
  hgvsp: ENSP00000430065.1:p.Glu233Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14251G>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14251G>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.769G>T
  hgvsp: ENSP00000430128.1:p.Glu257Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.730G>T
  hgvsp: ENSP00000430394.1:p.Glu244Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.730G>T
  hgvsp: ENSP00000428667.1:p.Glu244Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.511G>T
  hgvsp: ENSP00000428807.1:p.Glu171Ter
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.730G>T
  hgvsp: ENSP00000430367.1:p.Glu244Ter
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu257Ter
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/8-85799884-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799884
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799884
    reference: chr 8
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.698A>C
  hgvsp: ENSP00000430065.1:p.Glu233Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.512A>C
  hgvsp: ENSP00000428807.1:p.Glu171Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.731A>C
  hgvsp: ENSP00000428667.1:p.Glu244Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.731A>C
  hgvsp: ENSP00000430394.1:p.Glu244Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14252A>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.731A>C
  hgvsp: ENSP00000430367.1:p.Glu244Ala
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14252A>C
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.770A>C
  hgvsp: ENSP00000430128.1:p.Glu257Ala
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4867
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu257Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

8-85799888-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 85799888
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 85799888
    reference: chr 8
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428667
  ensembl transcript: ENST00000521695
  gene symbol: RALYL
  hgvsc: ENST00000521695.1:c.735A>T
  hgvsp: ENSP00000428667.1:p.Glu245Asp
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl transcript: ENST00000518065
  gene symbol: RALYL
  hgvsc: ENST00000518065.1:n.916+14256A>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428310
  ensembl transcript: ENST00000521376
  gene symbol: RALYL
  hgvsc: ENST00000521376.1:c.418+14256A>T
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430065
  ensembl transcript: ENST00000518566
  gene symbol: RALYL
  hgvsc: ENST00000518566.1:c.702A>T
  hgvsp: ENSP00000430065.1:p.Glu234Asp
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430128
  ensembl transcript: ENST00000517638
  gene symbol: RALYL
  hgvsc: ENST00000517638.1:c.774A>T
  hgvsp: ENSP00000430128.1:p.Glu258Asp
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000428807
  ensembl transcript: ENST00000523850
  gene symbol: RALYL
  hgvsc: ENST00000523850.1:c.516A>T
  hgvsp: ENSP00000428807.1:p.Glu172Asp
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430367
  ensembl transcript: ENST00000521268
  gene symbol: RALYL
  hgvsc: ENST00000521268.1:c.735A>T
  hgvsp: ENSP00000430367.1:p.Glu245Asp
  variant of: http://identifiers.org/hgnc/27036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184672
  ensembl protein: ENSP00000430394
  ensembl transcript: ENST00000522455
  gene symbol: RALYL
  hgvsc: ENST00000522455.1:c.735A>T
  hgvsp: ENSP00000430394.1:p.Glu245Asp
  variant of: http://identifiers.org/hgnc/27036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2443
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu258Asp
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33281
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1258
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3560
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2028
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4354
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.849114703618168e-4
allele num: 2598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24628
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.49805e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.311e0

FS
type: SiteQuality
SIO_000300: 2.158e0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

QD
type: SiteQuality
SIO_000300: 1.737e1

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 200
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 9.75e1
variant carriers: 32

GenotypeQuality
all individuals: 374
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 6.75e1
variant carriers: 1

East Asian
type: Population
allele count: 31
allele frequency: 1.018396846254928e-2
allele num: 3044
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27806
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

QD
type: SiteQuality
SIO_000300: 1.029e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 8.92116e5

VQSLOD
type: SiteQuality
SIO_000300: 2.97e0

GenotypeQuality
all individuals: 1162
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 319
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 3.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 2

GenotypeQuality
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bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 356
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 389
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2482
bin: 9.75e1
variant carriers: 59

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.914672935970129e-5
allele num: 28924
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3016
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 1.099706744868035e-3
allele num: 2728
num of homozygotes: 0

African
type: Population
allele count: 55
allele frequency: 1.114714227807053e-2
allele num: 4934
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3186
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.272727272727273e-3
allele num: 440
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.05648e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.493e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

FS
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

GenotypeQuality
all individuals: 890
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
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variant carriers: 0

GenotypeQuality
all individuals: 251
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GenotypeQuality
all individuals: 2541
bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3234
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.414367659109533e-5
allele num: 29288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3042
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.453e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.36e-1

QD
type: SiteQuality
SIO_000300: 7.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

DP
type: SiteQuality
SIO_000300: 9.07706e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.325e1

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
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variant carriers: 0

GenotypeQuality
all individuals: 31376
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GenotypeQuality
all individuals: 123
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GenotypeQuality
all individuals: 340
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variant carriers: 0

GenotypeQuality
all individuals: 2588
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GenotypeQuality
all individuals: 515
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GenotypeQuality
all individuals: 1304
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 4.75e1
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GenotypeQuality
all individuals: 350
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30044
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.10373e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

VQSLOD
type: SiteQuality
SIO_000300: -1.001e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

QD
type: SiteQuality
SIO_000300: 1.286e1

GenotypeQuality
all individuals: 1153
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.5e0
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GenotypeQuality
all individuals: 1044
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
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variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
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GenotypeQuality
all individuals: 1164
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
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variant carriers: 0

GenotypeQuality
all individuals: 402
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variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.645927974191849e-4
allele num: 30378
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 9.08584e5

FS
type: SiteQuality
SIO_000300: 4.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.72e0

VQSLOD
type: SiteQuality
SIO_000300: 5.46e-1

GenotypeQuality
all individuals: 530
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
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GenotypeQuality
all individuals: 246
bin: 4.25e1
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GenotypeQuality
all individuals: 1056
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
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GenotypeQuality
all individuals: 631
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GenotypeQuality
all individuals: 14299
bin: 6.25e1
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GenotypeQuality
all individuals: 446
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GenotypeQuality
all individuals: 2432
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 31616
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.302073702285035e-5
allele num: 30284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2930
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3054
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.023e0

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.399e0

QD
type: SiteQuality
SIO_000300: 1.314e1

DP
type: SiteQuality
SIO_000300: 9.0462e5

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.45e-1

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
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GenotypeQuality
all individuals: 551
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variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.5e0
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GenotypeQuality
all individuals: 526
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variant carriers: 0

GenotypeQuality
all individuals: 406
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GenotypeQuality
all individuals: 31904
bin: 2.25e1
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GenotypeQuality
all individuals: 2432
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 346
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GenotypeQuality
all individuals: 506
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GenotypeQuality
all individuals: 336
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GenotypeQuality
all individuals: 14560
bin: 6.25e1
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GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3042
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.001200480192077e-4
allele num: 3332
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30336
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.599e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.883e0

QD
type: SiteQuality
SIO_000300: 1.661e1

MQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.614e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

DP
type: SiteQuality
SIO_000300: 9.03615e5

GenotypeQuality
all individuals: 553
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.75e1
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GenotypeQuality
all individuals: 284
bin: 2.5e0
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GenotypeQuality
all individuals: 347
bin: 7.25e1
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GenotypeQuality
all individuals: 542
bin: 1.25e1
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GenotypeQuality
all individuals: 397
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GenotypeQuality
all individuals: 14039
bin: 6.25e1
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GenotypeQuality
all individuals: 1169
bin: 1.75e1
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GenotypeQuality
all individuals: 404
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GenotypeQuality
all individuals: 548
bin: 3.75e1
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GenotypeQuality
all individuals: 1141
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2432
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3044
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.317189676905725e-5
allele num: 30146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4998
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.554e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.9883e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

FS
type: SiteQuality
SIO_000300: 4.082e0

QD
type: SiteQuality
SIO_000300: 4.56e0

GenotypeQuality
all individuals: 159
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 562
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13542
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3324
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2437
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 405
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.333600053344002e-4
allele num: 29994
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3024
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.019e0

QD
type: SiteQuality
SIO_000300: 1.274e1

FS
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

DP
type: SiteQuality
SIO_000300: 8.94447e5

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1009
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3324
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2437
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 600
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9382
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.334000133360006e-5
allele num: 29994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3284
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.436426116838488e-4
allele num: 2910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3024
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.019e0

DP
type: SiteQuality
SIO_000300: 8.94447e5

FS
type: SiteQuality
SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 1.274e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

GenotypeQuality
all individuals: 1144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 379
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2432
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 399
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1139
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 507
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.321597023849066e-5
allele num: 30106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3036
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5014
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3318
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 8.92772e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.389e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 7.91e0

GenotypeQuality
all individuals: 4049
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12963
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32883
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.066098081023454e-4
allele num: 9380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4948
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.073e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

FS
type: SiteQuality
SIO_000300: 4.968e0

DP
type: SiteQuality
SIO_000300: 8.75447e5

VQSLOD
type: SiteQuality
SIO_000300: -2.153e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.898e0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

GenotypeQuality
all individuals: 390
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11385
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2946
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.017e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.113e0

DP
type: SiteQuality
SIO_000300: 8.57778e5

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.06e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 4.97e0

GenotypeQuality
all individuals: 32565
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 299
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 309
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 247
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 155
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1354
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2517
bin: 9.75e1
variant carriers: 93

GenotypeQuality
all individuals: 1039
bin: 6.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2698
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.105263157894737e-4
allele num: 4750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 91
allele frequency: 3.228095069173466e-3
allele num: 28190
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 2.28310502283105e-3
allele num: 438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2932
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.473e0

FS
type: SiteQuality
SIO_000300: 1.965e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

DP
type: SiteQuality
SIO_000300: 8.3924e5

QD
type: SiteQuality
SIO_000300: 1.258e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

GenotypeQuality
all individuals: 2431
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 812
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10053
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1672
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6324
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2914
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2874
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.33e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

DP
type: SiteQuality
SIO_000300: 8.2767e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

GenotypeQuality
all individuals: 446
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9290
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31715
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1644
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2431
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
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GenotypeQuality
all individuals: 928
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.965107057890563e-4
allele num: 2522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.719961312402351e-5
allele num: 26882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9084
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.361e0

QD
type: SiteQuality
SIO_000300: 4.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.61e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 7.464e0

DP
type: SiteQuality
SIO_000300: 8.09192e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.25e1
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GenotypeQuality
all individuals: 1168
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30341
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2678
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.829363559776365e-5
allele num: 26114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8986
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.081e1

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 7.88638e5

ClippingRankSum
type: SiteQuality
SIO_000300: -8.61e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.612e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.79e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.402e0

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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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2652
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8688
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 4.191817572099262e-5
allele num: 23856
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1912
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4256
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.14e-2

DP
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SIO_000300: 7.41002e5

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

BaseQRankSum
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SIO_000300: -7.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.68e-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
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1912
num of homozygotes: 0

East Asian
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allele count: 3
allele frequency: 1.270110076206604e-3
allele num: 2362
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8688
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2652
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 23856
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.639999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.14e-2

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

QD
type: SiteQuality
SIO_000300: 1.224e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

DP
type: SiteQuality
SIO_000300: 7.41002e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.18e-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: 2456
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1440
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.765535646206634e-5
allele num: 20984
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.038e-1

FS
type: SiteQuality
SIO_000300: 1.775e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.26e-2

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.789999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

DP
type: SiteQuality
SIO_000300: 6.83278e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3740
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8238
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 5.013033888109083e-5
allele num: 19948
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1732
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2384
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 6.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-1

FS
type: SiteQuality
SIO_000300: 2.963e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.49e-2

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e0

GenotypeQuality
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variant carriers: 1

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

African
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allele count: 1
allele frequency: 2.745744096650192e-4
allele num: 3642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1140
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 19200
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2340
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

QD
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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1520
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 332
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South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2300
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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DP
type: SiteQuality
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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

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

European (Finnish)
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East Asian
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num of homozygotes: 0

Latino
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African
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Other
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South Asian
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 6.29009938357026e-5
allele num: 15898
num of homozygotes: 0

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

European (Finnish)
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Other
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South Asian
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African
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East Asian
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European (Non-Finnish)
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allele frequency: 6.311537490532694e-5
allele num: 15844
num of homozygotes: 0

MQ
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.29e-2

QD
type: SiteQuality
SIO_000300: 8.68e0

VQSLOD
type: SiteQuality
SIO_000300: -2.912e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

DP
type: SiteQuality
SIO_000300: 6.07901e5

GenotypeQuality
all individuals: 2807
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11910
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23850
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 427
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541307028360049e-5
allele num: 64880
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.127e0

QD
type: SiteQuality
SIO_000300: 3.171e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.911e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 2.301e0

DP
type: SiteQuality
SIO_000300: 2.878039e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5160
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2820
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64884
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.464533604198409e-5
allele num: 11814
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.883154e6

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.196e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

VQSLOD
type: SiteQuality
SIO_000300: -1.582e0

MQ
type: SiteQuality
SIO_000300: 6.107e1

GenotypeQuality
all individuals: 5040
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4242
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3169
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11143
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2820
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1700
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2627
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11936
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540309910353963e-5
allele num: 64922
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 1.894e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.859e0

QD
type: SiteQuality
SIO_000300: 5.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

DP
type: SiteQuality
SIO_000300: 2.898255e6

VQSLOD
type: SiteQuality
SIO_000300: -4.726e-1

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6742
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8456
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2065
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3120
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23851
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.77963125548727e-5
allele num: 11390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64816
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.368e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e0

MQRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.387e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.68e-1

MQ
type: SiteQuality
SIO_000300: 5.997e1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

DP
type: SiteQuality
SIO_000300: 2.962618e6

GenotypeQuality
all individuals: 3118
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2627
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1700
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4972
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1835
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23855
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2778
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2971
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.623956607879438e-5
allele num: 61578
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

DP
type: SiteQuality
SIO_000300: 3.188073e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.77e-1

QD
type: SiteQuality
SIO_000300: 1.951e1

VQSLOD
type: SiteQuality
SIO_000300: 2.88e0

FS
type: SiteQuality
SIO_000300: 1.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.49e-1

MQ
type: SiteQuality
SIO_000300: 6.048e1

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.520681265206813e-4
allele num: 6576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64518
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.239e-1

MQ
type: SiteQuality
SIO_000300: 6.012e1

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.55e0

DP
type: SiteQuality
SIO_000300: 3.846125e6

QD
type: SiteQuality
SIO_000300: 1.612e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

GenotypeQuality
all individuals: 304
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1279
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 1183
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1149
bin: 8.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1240
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 412
bin: 5.75e1
variant carriers: 9

GenotypeQuality
all individuals: 342
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 371
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 1577
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 989
bin: 8.75e1
variant carriers: 12

GenotypeQuality
all individuals: 391
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 955
bin: 2.25e1
variant carriers: 7

Other
type: Population
allele count: 19
allele frequency: 2.214452214452214e-2
allele num: 858
num of homozygotes: 1

East Asian
type: Population
allele count: 227
allele frequency: 2.652488899275532e-2
allele num: 8558
num of homozygotes: 2

Latino
type: Population
allele count: 904
allele frequency: 8.001416179854842e-2
allele num: 11298
num of homozygotes: 23

African
type: Population
allele count: 40
allele frequency: 4.112687641373638e-3
allele num: 9726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1089
allele frequency: 1.687901050869525e-2
allele num: 64518
num of homozygotes: 3

South Asian
type: Population
allele count: 136
allele frequency: 1.035322777101096e-2
allele num: 13136
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 68
allele frequency: 1.034063260340633e-2
allele num: 6576
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.012e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.239e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

DP
type: SiteQuality
SIO_000300: 3.846125e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

QD
type: SiteQuality
SIO_000300: 1.612e1

FS
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeQuality
all individuals: 371
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45991
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 989
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.394959546173161e-4
allele num: 64518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.505491937368544e-4
allele num: 8558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.239e-1

DP
type: SiteQuality
SIO_000300: 3.846125e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.55e0

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

MQ
type: SiteQuality
SIO_000300: 6.012e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

QD
type: SiteQuality
SIO_000300: 1.612e1

GenotypeQuality
all individuals: 1149
bin: 8.25e1
variant carriers: 139

GenotypeQuality
all individuals: 45991
bin: 9.75e1
variant carriers: 33945

GenotypeQuality
all individuals: 342
bin: 7.5e0
variant carriers: 40

GenotypeQuality
all individuals: 1240
bin: 6.75e1
variant carriers: 123

GenotypeQuality
all individuals: 304
bin: 1.75e1
variant carriers: 58

GenotypeQuality
all individuals: 1279
bin: 2.5e0
variant carriers: 33

GenotypeQuality
all individuals: 391
bin: 4.25e1
variant carriers: 130

GenotypeQuality
all individuals: 455
bin: 2.75e1
variant carriers: 60

GenotypeQuality
all individuals: 1196
bin: 9.25e1
variant carriers: 174

GenotypeQuality
all individuals: 497
bin: 3.25e1
variant carriers: 96

GenotypeQuality
all individuals: 989
bin: 8.75e1
variant carriers: 167

GenotypeQuality
all individuals: 1577
bin: 6.25e1
variant carriers: 157

African
type: Population
allele count: 6763
allele frequency: 6.953526629652478e-1
allele num: 9726
num of homozygotes: 2321

European (Finnish)
type: Population
allele count: 2253
allele frequency: 3.426094890510949e-1
allele num: 6576
num of homozygotes: 390

South Asian
type: Population
allele count: 4608
allele frequency: 3.507917174177832e-1
allele num: 13136
num of homozygotes: 722

East Asian
type: Population
allele count: 6285
allele frequency: 7.3440056087871e-1
allele num: 8558
num of homozygotes: 2291

Latino
type: Population
allele count: 5200
allele frequency: 4.602584528235086e-1
allele num: 11298
num of homozygotes: 1163

Other
type: Population
allele count: 327
allele frequency: 3.811188811188811e-1
allele num: 858
num of homozygotes: 67

European (Non-Finnish)
type: Population
allele count: 20073
allele frequency: 3.11122477448154e-1
allele num: 64518
num of homozygotes: 3056

MQ
type: SiteQuality
SIO_000300: 6.012e1

QD
type: SiteQuality
SIO_000300: 1.612e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.239e-1

DP
type: SiteQuality
SIO_000300: 3.846125e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.55e0

GenotypeQuality
all individuals: 391
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45991
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 1240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 8.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 2
allele frequency: 2.336994624912363e-4
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.112687641373637e-4
allele num: 9726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 9.896467722289889e-4
allele num: 13136
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.165501165501166e-3
allele num: 858
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.239e-1

QD
type: SiteQuality
SIO_000300: 1.612e1

VQSLOD
type: SiteQuality
SIO_000300: 5.55e0

DP
type: SiteQuality
SIO_000300: 3.846125e6

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

MQ
type: SiteQuality
SIO_000300: 6.012e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

GenotypeQuality
all individuals: 1009
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.538320005661312e-5
allele num: 28262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2772
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2256
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.14e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.087e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

FS
type: SiteQuality
SIO_000300: 2.84e0

QD
type: SiteQuality
SIO_000300: 1.002e1

DP
type: SiteQuality
SIO_000300: 1.199974e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

GenotypeQuality
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bin: 1.25e1
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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.670564650851988e-4
allele num: 5986
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 2.119927316777711e-3
allele num: 3302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31228
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

FS
type: SiteQuality
SIO_000300: 6.211e0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

MQ
type: SiteQuality
SIO_000300: 6.012e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.821e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-2

QD
type: SiteQuality
SIO_000300: 1.591e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.016e0

DP
type: SiteQuality
SIO_000300: 4.106035e6

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

GenotypeQuality
all individuals: 157
bin: 1.75e1
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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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: 330
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12462
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5986
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2878
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.165501165501166e-3
allele num: 858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.012e1

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.821e0

FS
type: SiteQuality
SIO_000300: 6.211e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

DP
type: SiteQuality
SIO_000300: 4.106035e6

QD
type: SiteQuality
SIO_000300: 1.591e1

VQSLOD
type: SiteQuality
SIO_000300: -1.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

GenotypeQuality
all individuals: 38932
bin: 9.75e1
variant carriers: 12

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 3461
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.537205081669691e-4
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.361779391738538e-4
allele num: 66090
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

DP
type: SiteQuality
SIO_000300: 3.268452e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.858e0

FS
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

QD
type: SiteQuality
SIO_000300: 1.316e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38932
bin: 9.75e1
variant carriers: 7

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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3461
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.052352852171281e-5
allele num: 66090
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: 2
allele frequency: 1.736111111111111e-4
allele num: 11520
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.749460043196545e-5
allele num: 14816
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

FS
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

QD
type: SiteQuality
SIO_000300: 1.316e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.858e0

DP
type: SiteQuality
SIO_000300: 3.268452e6

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51308821304282e-5
allele num: 66090
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 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: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.316e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.858e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-2

FS
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

DP
type: SiteQuality
SIO_000300: 3.268452e6

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511350240304688e-5
allele num: 66166
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15042
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.998e1

DP
type: SiteQuality
SIO_000300: 3.267845e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.92e-1

FS
type: SiteQuality
SIO_000300: 4.771e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.046e0

MQRankSum
type: SiteQuality
SIO_000300: -1.21e-1

QD
type: SiteQuality
SIO_000300: 1.111e1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.569373072970195e-4
allele num: 66164
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: 0
allele frequency: 0.0e0
allele num: 15084
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

QD
type: SiteQuality
SIO_000300: 1.174e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.516e0

MQRankSum
type: SiteQuality
SIO_000300: -4.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.268672e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.14e-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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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 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: 8600
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African
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allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.988862370723946e-4
allele num: 15084
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.534187775829756e-5
allele num: 66164
num of homozygotes: 0

DP
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InbreedingCoeff
type: SiteQuality
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QD
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: -4.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-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

GenotypeQuality
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variant carriers: 4

South Asian
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allele frequency: 0.0e0
allele num: 15084
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 8.680555555555556e-5
allele num: 11520
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.022791850553171e-5
allele num: 66164
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
type: SiteQuality
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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QD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511258878645912e-5
allele num: 66170
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.604618857440528e-4
allele num: 11518
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9786
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.321877065432915e-4
allele num: 15130
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ClippingRankSum
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SIO_000300: -7.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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SIO_000300: 1.31e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.269765e6

QD
type: SiteQuality
SIO_000300: 1.182e1

GenotypeQuality
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variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
allele frequency: 2.323420074349442e-4
allele num: 8608
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15130
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511258878645912e-5
allele num: 66170
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

BaseQRankSum
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SIO_000300: -2.165e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

FS
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 3.269765e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.021867974657674e-4
allele num: 9786
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15130
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.266888317968868e-4
allele num: 66170
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.182e1

DP
type: SiteQuality
SIO_000300: 3.269765e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.165e0

FS
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e-1

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

European (Non-Finnish)
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allele count: 9
allele frequency: 1.360132990781321e-4
allele num: 66170
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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Latino
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allele count: 2
allele frequency: 1.736412571627018e-4
allele num: 11518
num of homozygotes: 0

South Asian
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allele frequency: 1.321877065432915e-4
allele num: 15130
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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DP
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Other
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allele num: 888
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East Asian
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South Asian
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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Other
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East Asian
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 2.605071205279611e-4
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66212
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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ClippingRankSum
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MQ
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FS
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.416480396302785e-4
allele num: 66212
num of homozygotes: 0

Latino
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allele frequency: 6.946856547412296e-4
allele num: 11516
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 59
allele frequency: 6.031486403598446e-3
allele num: 9782
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East Asian
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allele frequency: 1.163061177017911e-4
allele num: 8598
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South Asian
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allele frequency: 4.613762193514369e-4
allele num: 15172
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VQSLOD
type: SiteQuality
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MQ
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.38e-2

FS
type: SiteQuality
SIO_000300: 1.303e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.456e0

DP
type: SiteQuality
SIO_000300: 3.272688e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

QD
type: SiteQuality
SIO_000300: 1.326e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.041200990756963e-5
allele num: 66212
num of homozygotes: 0

African
type: Population
allele count: 70
allele frequency: 7.156000817828665e-3
allele num: 9782
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.272688e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

FS
type: SiteQuality
SIO_000300: 1.303e0

QD
type: SiteQuality
SIO_000300: 1.326e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.456e0

GenotypeQuality
all individuals: 1123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.25e1
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GenotypeQuality
all individuals: 2381
bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 3.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 33

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 4038
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.126126126126126e-3
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.531448250860975e-5
allele num: 66204
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.045782012549384e-3
allele num: 8606
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: 11518
num of homozygotes: 0

South Asian
type: Population
allele count: 21
allele frequency: 1.38194261647802e-3
allele num: 15196
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.131e0

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 2.084e0

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

QD
type: SiteQuality
SIO_000300: 1.249e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.268517e6

GenotypeQuality
all individuals: 2435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 227
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GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 610
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variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4038
bin: 6.25e1
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: 8606
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66204
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.580679126085812e-5
allele num: 15196
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.131e0

FS
type: SiteQuality
SIO_000300: 2.084e0

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

QD
type: SiteQuality
SIO_000300: 1.249e1

DP
type: SiteQuality
SIO_000300: 3.268517e6

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
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variant carriers: 0

GenotypeQuality
all individuals: 4038
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variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 302
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 2435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
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variant carriers: 0

GenotypeQuality
all individuals: 38952
bin: 9.75e1
variant carriers: 11

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

South Asian
type: Population
allele count: 6
allele frequency: 3.948407475651487e-4
allele num: 15196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020965500573983e-5
allele num: 66204
num of homozygotes: 0

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

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

African
type: Population
allele count: 3
allele frequency: 3.067484662576687e-4
allele num: 9780
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

QD
type: SiteQuality
SIO_000300: 1.249e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.084e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.131e0

DP
type: SiteQuality
SIO_000300: 3.268517e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

GenotypeQuality
all individuals: 1583
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 641
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variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
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variant carriers: 0

GenotypeQuality
all individuals: 610
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GenotypeQuality
all individuals: 2381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 9.25e1
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GenotypeQuality
all individuals: 4038
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66204
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.580679126085812e-5
allele num: 15196
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.022494887525562e-4
allele num: 9780
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.084e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.131e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

QD
type: SiteQuality
SIO_000300: 1.249e1

DP
type: SiteQuality
SIO_000300: 3.268517e6

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38926
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 661
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variant carriers: 0

GenotypeQuality
all individuals: 1091
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GenotypeQuality
all individuals: 2436
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variant carriers: 0

GenotypeQuality
all individuals: 156
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GenotypeQuality
all individuals: 1667
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2409
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 2709
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 7.75e1
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: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510254628930438e-5
allele num: 66214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 4.631e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

DP
type: SiteQuality
SIO_000300: 3.267974e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.142e0

QD
type: SiteQuality
SIO_000300: 1.2e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
SIO_000300: 6.014e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 470
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variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
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variant carriers: 0

GenotypeQuality
all individuals: 620
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variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2409
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3894
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 7.75e1
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: 0
allele frequency: 0.0e0
allele num: 15204
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.022285831118381e-4
allele num: 9782
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66214
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.2e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

DP
type: SiteQuality
SIO_000300: 3.267974e6

MQ
type: SiteQuality
SIO_000300: 6.014e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.142e0

FS
type: SiteQuality
SIO_000300: 4.631e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 528
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.015772490123345e-5
allele num: 66318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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: 11524
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.749e0

MQ
type: SiteQuality
SIO_000300: 6.091e1

DP
type: SiteQuality
SIO_000300: 3.274062e6

MQRankSum
type: SiteQuality
SIO_000300: -8.87e-1

QD
type: SiteQuality
SIO_000300: 1.097e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 3.473e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.535e0

GenotypeQuality
all individuals: 2500
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5370
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GenotypeQuality
all individuals: 185
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15566
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.677542519958348e-5
allele num: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66320
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: 9790
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.274981e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 3.742e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.06e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

MQ
type: SiteQuality
SIO_000300: 5.991e1

QD
type: SiteQuality
SIO_000300: 8.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 38887
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1669
bin: 8.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66392
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.313e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.742e0

VQSLOD
type: SiteQuality
SIO_000300: -6.421e-1

FS
type: SiteQuality
SIO_000300: 3.365e0

DP
type: SiteQuality
SIO_000300: 3.283001e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.56e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-1

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

GenotypeQuality
all individuals: 2720
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 196
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2453
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.513721714010592e-5
allele num: 66464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16030
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.292142e6

QD
type: SiteQuality
SIO_000300: 1.23e1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.127e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 4.912e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1620
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.169792694965449e-5
allele num: 16208
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: 11528
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.228e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 7.0e-1

DP
type: SiteQuality
SIO_000300: 3.296507e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.008712633318311e-5
allele num: 66570
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.53e-1

DP
type: SiteQuality
SIO_000300: 3.301405e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.515e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.512e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e0

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

GenotypeQuality
all individuals: 38888
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 2.5e0
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 2446
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.485e1

FS
type: SiteQuality
SIO_000300: 3.142e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.042e0

VQSLOD
type: SiteQuality
SIO_000300: 7.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 3.302675e6

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 2682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7607
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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: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: -3.818e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.004e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

QD
type: SiteQuality
SIO_000300: 7.1e-1

MQ
type: SiteQuality
SIO_000300: 5.997e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 3.302878e6

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 6.75e1
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GenotypeQuality
all individuals: 2397
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0