6-56368837-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368837
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368837
    reference: chr 6
allele count: 1
allele frequency: 8.504269143109841e-6
allele num: 117588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17919A>T
  hgvsp: ENST00000446842.2:c.17919A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18564A>T
  hgvsp: ENST00000361203.3:c.18564A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6235A>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12633A>T
  hgvsp: ENST00000421834.2:c.12633A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11655A>T
  hgvsp: ENST00000244364.6:c.11655A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3297A>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18897A>T
  hgvsp: ENST00000370769.4:c.18897A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12306A>T
  hgvsp: ENST00000370788.2:c.12306A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19431A>T
  hgvsp: ENST00000370754.5:c.19431A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly3885Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

6-56368841-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368841
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368841
    reference: chr 6
allele count: 2
allele frequency: 1.700882758151481e-5
allele num: 117586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17915T>C
  hgvsp: ENSP00000393645.2:p.Ile5972Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11651T>C
  hgvsp: ENSP00000244364.6:p.Ile3884Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12302T>C
  hgvsp: ENSP00000359824.2:p.Ile4101Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12629T>C
  hgvsp: ENSP00000400883.2:p.Ile4210Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18560T>C
  hgvsp: ENSP00000354508.3:p.Ile6187Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18893T>C
  hgvsp: ENSP00000359805.4:p.Ile6298Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19427T>C
  hgvsp: ENSP00000359790.5:p.Ile6476Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6231T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3293T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile3884Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

6-56368851-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368851
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368851
    reference: chr 6
allele count: 1
allele frequency: 8.497909514259493e-6
allele num: 117676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12619A>G
  hgvsp: ENSP00000400883.2:p.Met4207Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12292A>G
  hgvsp: ENSP00000359824.2:p.Met4098Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11641A>G
  hgvsp: ENSP00000244364.6:p.Met3881Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3283A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19417A>G
  hgvsp: ENSP00000359790.5:p.Met6473Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18550A>G
  hgvsp: ENSP00000354508.3:p.Met6184Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6221A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18883A>G
  hgvsp: ENSP00000359805.4:p.Met6295Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17905A>G
  hgvsp: ENSP00000393645.2:p.Met5969Val
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met3881Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

6-56368852-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368852
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368852
    reference: chr 6
allele count: 1
allele frequency: 8.49689863199932e-6
allele num: 117690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12291A>G
  hgvsp: ENST00000370788.2:c.12291A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12618A>G
  hgvsp: ENST00000421834.2:c.12618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19416A>G
  hgvsp: ENST00000370754.5:c.19416A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18549A>G
  hgvsp: ENST00000361203.3:c.18549A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3282A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11640A>G
  hgvsp: ENST00000244364.6:c.11640A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6220A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17904A>G
  hgvsp: ENST00000446842.2:c.17904A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18882A>G
  hgvsp: ENST00000370769.4:c.18882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1884
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser3880Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD

6-56368858-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368858
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368858
    reference: chr 6
allele count: 1
allele frequency: 8.500799075113061e-6
allele num: 117636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17898A>G
  hgvsp: ENST00000446842.2:c.17898A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12285A>G
  hgvsp: ENST00000370788.2:c.12285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3276A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18543A>G
  hgvsp: ENST00000361203.3:c.18543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19410A>G
  hgvsp: ENST00000370754.5:c.19410A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11634A>G
  hgvsp: ENST00000244364.6:c.11634A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12612A>G
  hgvsp: ENST00000421834.2:c.12612A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6214A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18876A>G
  hgvsp: ENST00000370769.4:c.18876A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43330
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5010
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu3878Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

6-56368862-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368862
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368862
    reference: chr 6
allele count: 1
allele frequency: 8.509624385179638e-6
allele num: 117514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12608A>G
  hgvsp: ENSP00000400883.2:p.Lys4203Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12281A>G
  hgvsp: ENSP00000359824.2:p.Lys4094Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3272A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18539A>G
  hgvsp: ENSP00000354508.3:p.Lys6180Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6210A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17894A>G
  hgvsp: ENSP00000393645.2:p.Lys5965Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19406A>G
  hgvsp: ENSP00000359790.5:p.Lys6469Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11630A>G
  hgvsp: ENSP00000244364.6:p.Lys3877Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18872A>G
  hgvsp: ENSP00000359805.4:p.Lys6291Arg
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3711
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys3877Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

6-56368865-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368865
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368865
    reference: chr 6
allele count: 1
allele frequency: 8.519193743504115e-6
allele num: 117382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18869G>C
  hgvsp: ENSP00000359805.4:p.Gly6290Ala
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18536G>C
  hgvsp: ENSP00000354508.3:p.Gly6179Ala
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3269G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6207G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12278G>C
  hgvsp: ENSP00000359824.2:p.Gly4093Ala
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19403G>C
  hgvsp: ENSP00000359790.5:p.Gly6468Ala
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11627G>C
  hgvsp: ENSP00000244364.6:p.Gly3876Ala
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12605G>C
  hgvsp: ENSP00000400883.2:p.Gly4202Ala
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17891G>C
  hgvsp: ENSP00000393645.2:p.Gly5964Ala
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2257
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly3876Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/6-56368866-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368866
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368866
    reference: chr 6
allele count: 1
allele frequency: 8.522243054371911e-6
allele num: 117340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19402G>T
  hgvsp: ENSP00000359790.5:p.Gly6468Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18535G>T
  hgvsp: ENSP00000354508.3:p.Gly6179Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11626G>T
  hgvsp: ENSP00000244364.6:p.Gly3876Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18868G>T
  hgvsp: ENSP00000359805.4:p.Gly6290Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17890G>T
  hgvsp: ENSP00000393645.2:p.Gly5964Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6206G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12277G>T
  hgvsp: ENSP00000359824.2:p.Gly4093Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3268G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12604G>T
  hgvsp: ENSP00000400883.2:p.Gly4202Cys
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly3876Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

6-56368891-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368891
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368891
    reference: chr 6
allele count: 6
allele frequency: 5.240357741755171e-5
allele num: 114496
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11601A>G
  hgvsp: ENST00000244364.6:c.11601A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19377A>G
  hgvsp: ENST00000370754.5:c.19377A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6181A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17865A>G
  hgvsp: ENST00000446842.2:c.17865A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18510A>G
  hgvsp: ENST00000361203.3:c.18510A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12579A>G
  hgvsp: ENST00000421834.2:c.12579A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12252A>G
  hgvsp: ENST00000370788.2:c.12252A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3243A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18843A>G
  hgvsp: ENST00000370769.4:c.18843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33016
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38082
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val3867Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

6-56368894-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368894
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368894
    reference: chr 6
allele count: 2
allele frequency: 1.757283941939339e-5
allele num: 113812
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3240G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12576G>A
  hgvsp: ENST00000421834.2:c.12576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11598G>A
  hgvsp: ENST00000244364.6:c.11598G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12249G>A
  hgvsp: ENST00000370788.2:c.12249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18840G>A
  hgvsp: ENST00000370769.4:c.18840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17862G>A
  hgvsp: ENST00000446842.2:c.17862G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19374G>A
  hgvsp: ENST00000370754.5:c.19374G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18507G>A
  hgvsp: ENST00000361203.3:c.18507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6178G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31878
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5949
  bin: 2.25e1
  variant carriers: 0
hgvs: c.11598G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

6-56368895-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368895
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368895
    reference: chr 6
allele count: 1
allele frequency: 8.804987144718768e-6
allele num: 113572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19373C>T
  hgvsp: ENSP00000359790.5:p.Ala6458Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11597C>T
  hgvsp: ENSP00000244364.6:p.Ala3866Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18839C>T
  hgvsp: ENSP00000359805.4:p.Ala6280Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12575C>T
  hgvsp: ENSP00000400883.2:p.Ala4192Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6177C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17861C>T
  hgvsp: ENSP00000393645.2:p.Ala5954Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18506C>T
  hgvsp: ENSP00000354508.3:p.Ala6169Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12248C>T
  hgvsp: ENSP00000359824.2:p.Ala4083Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3239C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala3866Val
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

6-56368903-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368903
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368903
    reference: chr 6
allele count: 1
allele frequency: 8.98908724808083e-6
allele num: 111246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-7C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-7C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-7C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-7C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-7C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-7C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-7C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-7C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-7C>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 7.25e1
  variant carriers: 0
hgvs: c.11596-7C>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

6-56368909-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368909
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368909
    reference: chr 6
allele count: 1
allele frequency: 9.154826424490992e-6
allele num: 109232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-13A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-13A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-13A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-13A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-13A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-13A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-13A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-13A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-13A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3493
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

6-56368911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368911
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368911
    reference: chr 6
allele count: 1
allele frequency: 9.192528312987204e-6
allele num: 108784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-15G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-15G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-15G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-15G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-15G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-15G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-15G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-15G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-15G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11863
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5010
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

6-56368912-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368912
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368912
    reference: chr 6
allele count: 1
allele frequency: 9.221689413500553e-6
allele num: 108440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-16C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-16C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-16C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-16C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-16C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-16C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-16C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-16C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-16C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13276
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5006
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3272
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/6-56368915-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368915
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368915
    reference: chr 6
allele count: 22
allele frequency: 2.041725443611255e-4
allele num: 107752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-19G>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15188
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18758
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7511
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3766
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4579
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

6-56368917-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368917
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368917
    reference: chr 6
allele count: 5
allele frequency: 4.67106369462454e-5
allele num: 107042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-21G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-21G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-21G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-21G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-21G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-21G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-21G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-21G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-21G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16602
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16923
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2205
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19069
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

6-56368918-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368918
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368918
    reference: chr 6
allele count: 8
allele frequency: 7.485730326564986e-5
allele num: 106870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-22C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-22C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-22C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-22C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-22C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-22C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-22C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-22C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-22C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6935
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16865
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 872
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5220
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

6-56368933-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368933
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368933
    reference: chr 6
allele count: 1
allele frequency: 9.70817233947537e-6
allele num: 103006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-37A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-37A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-37A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-37A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-37A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-37A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-37A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-37A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-37A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7933
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14026
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1834
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

6-56368936-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368936
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368936
    reference: chr 6
allele count: 10
allele frequency: 9.811231898277148e-5
allele num: 101924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-40T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-40T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-40T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-40T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-40T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-40T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-40T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-40T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-40T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12981
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7357
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5249
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2367
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7388
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

6-56368937-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368937
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368937
    reference: chr 6
allele count: 1
allele frequency: 9.865435460321219e-6
allele num: 101364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-41A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-41A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-41A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-41A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-41A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-41A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-41A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-41A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-41A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2627
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6795
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

6-56368938-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368938
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368938
    reference: chr 6
allele count: 1
allele frequency: 9.949060808659663e-6
allele num: 100512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-42A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6345
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2917
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2301
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-56368942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368942
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368942
    reference: chr 6
allele count: 1
allele frequency: 1.007698818976984e-5
allele num: 99236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-46T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-46T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-46T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-46T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-46T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-46T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-46T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-46T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-46T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12701
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11628
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5005
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4978
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

6-56368946-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56368946
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56368946
    reference: chr 6
allele count: 2
allele frequency: 2.064324346641344e-5
allele num: 96884
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17860-50C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11596-50C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12247-50C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3238-50C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18838-50C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6176-50C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19372-50C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12574-50C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18505-50C>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17899
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5006
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1504
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

6-56371192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371192
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371192
    reference: chr 6
allele count: 3
allele frequency: 4.211826809681586e-5
allele num: 71228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+49G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+49G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+49G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+49G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+49G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+49G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+49G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+49G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+49G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19673
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2417
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4349
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5765
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

6-56371193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371193
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371193
    reference: chr 6
allele count: 5
allele frequency: 6.953135864274787e-5
allele num: 71910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+48C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+48C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+48C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+48C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+48C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+48C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+48C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+48C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+48C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19736
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2249
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2034
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3935
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4352
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

6-56371197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371197
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371197
    reference: chr 6
allele count: 1
allele frequency: 1.376348821845408e-5
allele num: 72656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+44G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+44G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+44G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+44G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+44G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+44G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+44G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+44G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+44G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19768
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5899
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4347
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4297
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1928
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/6-56371214-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371214
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371214
    reference: chr 6
allele count: 1
allele frequency: 1.270260657486916e-5
allele num: 78724
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+27G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+27G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+27G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+27G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+27G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+27G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+27G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+27G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+27G>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13417
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3545
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13213
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

6-56371214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371214
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371214
    reference: chr 6
allele count: 11
allele frequency: 1.397286723235608e-4
allele num: 78724
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+27G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+27G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+27G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+27G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+27G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+27G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+27G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+27G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+27G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13417
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15250
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19276
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13213
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4358
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 19450
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

6-56371216-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371216
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371216
    reference: chr 6
allele count: 1
allele frequency: 1.243502698400856e-5
allele num: 80418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+25T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+25T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+25T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+25T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+25T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+25T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+25T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+25T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+25T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4898
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19167
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15434
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

6-56371217-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371217
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371217
    reference: chr 6
allele count: 2
allele frequency: 2.479236395190281e-5
allele num: 80670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+24C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+24C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+24C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+24C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+24C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+24C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+24C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+24C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+24C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13649
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15778
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15700
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4350
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3094
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

6-56371219-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371219
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371219
    reference: chr 6
allele count: 1
allele frequency: 1.209014411451784e-5
allele num: 82712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+22T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+22T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+22T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+22T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+22T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+22T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+22T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+22T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+22T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17452
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17387
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4491
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

6-56371220-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371220
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371220
    reference: chr 6
allele count: 7
allele frequency: 8.41629394507767e-5
allele num: 83172
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+21G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+21G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+21G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+21G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+21G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+21G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+21G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+21G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+21G>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12109
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18138
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5094
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4362
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

6-56371221-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371221
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371221
    reference: chr 6
allele count: 1
allele frequency: 1.191100100052408e-5
allele num: 83956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+20T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11796
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-56371225-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371225
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371225
    reference: chr 6
allele count: 2
allele frequency: 2.300966405890474e-5
allele num: 86920
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+16T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+16T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+16T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+16T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+16T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+16T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+16T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+16T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+16T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16062
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21750
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3669
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

6-56371236-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371236
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371236
    reference: chr 6
allele count: 1
allele frequency: 1.042665888142803e-5
allele num: 95908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12246+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19371+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11595+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17859+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18504+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3237+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6175+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12573+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18837+5G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28961
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
hgvs: c.11595+5G>A
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD

6-56371265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371265
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371265
    reference: chr 6
allele count: 1
allele frequency: 9.082157193976713e-6
allele num: 110106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19347C>T
  hgvsp: ENST00000370754.5:c.19347C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17835C>T
  hgvsp: ENST00000446842.2:c.17835C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12222C>T
  hgvsp: ENST00000370788.2:c.12222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11571C>T
  hgvsp: ENST00000244364.6:c.11571C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6151C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12549C>T
  hgvsp: ENST00000421834.2:c.12549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18813C>T
  hgvsp: ENST00000370769.4:c.18813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18480C>T
  hgvsp: ENST00000361203.3:c.18480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3213C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala3857Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-56371268-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371268
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371268
    reference: chr 6
allele count: 1
allele frequency: 9.022990579997834e-6
allele num: 110828
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18477T>G
  hgvsp: ENST00000361203.3:c.18477T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12219T>G
  hgvsp: ENST00000370788.2:c.12219T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19344T>G
  hgvsp: ENST00000370754.5:c.19344T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17832T>G
  hgvsp: ENST00000446842.2:c.17832T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11568T>G
  hgvsp: ENST00000244364.6:c.11568T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12546T>G
  hgvsp: ENST00000421834.2:c.12546T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6148T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18810T>G
  hgvsp: ENST00000370769.4:c.18810T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3210T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala3856Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-56371270-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371270
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371270
    reference: chr 6
allele count: 1
allele frequency: 9.007548325496767e-6
allele num: 111018
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11566G>T
  hgvsp: ENSP00000244364.6:p.Ala3856Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19342G>T
  hgvsp: ENSP00000359790.5:p.Ala6448Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12217G>T
  hgvsp: ENSP00000359824.2:p.Ala4073Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18475G>T
  hgvsp: ENSP00000354508.3:p.Ala6159Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3208G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17830G>T
  hgvsp: ENSP00000393645.2:p.Ala5944Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12544G>T
  hgvsp: ENSP00000400883.2:p.Ala4182Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18808G>T
  hgvsp: ENSP00000359805.4:p.Ala6270Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6146G>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1042
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala3856Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-56371276-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371276
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371276
    reference: chr 6
allele count: 1
allele frequency: 8.920606601248886e-6
allele num: 112100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6140A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12211A>G
  hgvsp: ENSP00000359824.2:p.Met4071Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19336A>G
  hgvsp: ENSP00000359790.5:p.Met6446Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11560A>G
  hgvsp: ENSP00000244364.6:p.Met3854Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18469A>G
  hgvsp: ENSP00000354508.3:p.Met6157Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3202A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12538A>G
  hgvsp: ENSP00000400883.2:p.Met4180Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18802A>G
  hgvsp: ENSP00000359805.4:p.Met6268Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17824A>G
  hgvsp: ENSP00000393645.2:p.Met5942Val
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met3854Val
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: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-56371286-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371286
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371286
    reference: chr 6
allele count: 1
allele frequency: 8.853318223670232e-6
allele num: 112952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12201T>G
  hgvsp: ENST00000370788.2:c.12201T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12528T>G
  hgvsp: ENST00000421834.2:c.12528T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18792T>G
  hgvsp: ENST00000370769.4:c.18792T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17814T>G
  hgvsp: ENST00000446842.2:c.17814T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18459T>G
  hgvsp: ENST00000361203.3:c.18459T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19326T>G
  hgvsp: ENST00000370754.5:c.19326T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11550T>G
  hgvsp: ENST00000244364.6:c.11550T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3192T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6130T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40448
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu3850Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-56371296-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371296
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371296
    reference: chr 6
allele count: 1
allele frequency: 8.827839474566994e-6
allele num: 113278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19316T>C
  hgvsp: ENSP00000359790.5:p.Ile6439Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18782T>C
  hgvsp: ENSP00000359805.4:p.Ile6261Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12518T>C
  hgvsp: ENSP00000400883.2:p.Ile4173Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17804T>C
  hgvsp: ENSP00000393645.2:p.Ile5935Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11540T>C
  hgvsp: ENSP00000244364.6:p.Ile3847Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18449T>C
  hgvsp: ENSP00000354508.3:p.Ile6150Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12191T>C
  hgvsp: ENSP00000359824.2:p.Ile4064Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6120T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3182T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile3847Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

6-56371299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371299
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371299
    reference: chr 6
allele count: 2
allele frequency: 1.766503559504672e-5
allele num: 113218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3179G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12188G>A
  hgvsp: ENSP00000359824.2:p.Arg4063Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18779G>A
  hgvsp: ENSP00000359805.4:p.Arg6260Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18446G>A
  hgvsp: ENSP00000354508.3:p.Arg6149Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17801G>A
  hgvsp: ENSP00000393645.2:p.Arg5934Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6117G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19313G>A
  hgvsp: ENSP00000359790.5:p.Arg6438Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11537G>A
  hgvsp: ENSP00000244364.6:p.Arg3846Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12515G>A
  hgvsp: ENSP00000400883.2:p.Arg4172Gln
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg3846Gln
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

6-56371304-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371304
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371304
    reference: chr 6
allele count: 1
allele frequency: 8.855983988380948e-6
allele num: 112918
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18441A>G
  hgvsp: ENST00000361203.3:c.18441A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6112A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19308A>G
  hgvsp: ENST00000370754.5:c.19308A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12183A>G
  hgvsp: ENST00000370788.2:c.12183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12510A>G
  hgvsp: ENST00000421834.2:c.12510A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11532A>G
  hgvsp: ENST00000244364.6:c.11532A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3174A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17796A>G
  hgvsp: ENST00000446842.2:c.17796A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18774A>G
  hgvsp: ENST00000370769.4:c.18774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5517
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys3844Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

6-56371360-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371360
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371360
    reference: chr 6
allele count: 2
allele frequency: 1.874519654338576e-5
allele num: 106694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6074-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18403-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12472-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12145-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3136-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19270-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11494-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17758-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18736-18C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14081
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17546
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11096
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-56371360-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371360
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371360
    reference: chr 6
allele count: 2
allele frequency: 1.874519654338576e-5
allele num: 106694
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18736-18C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6074-18C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17758-18C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11494-18C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3136-18C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19270-18C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18403-18C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12472-18C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12145-18C>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4374
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11096
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

6-56371369-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371369
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371369
    reference: chr 6
allele count: 1
allele frequency: 9.475439660400243e-6
allele num: 105536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12145-27A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19270-27A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12472-27A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11494-27A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3136-27A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17758-27A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18403-27A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18736-27A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6074-27A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15319
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4332
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2213
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6607
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

6-56371371-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371371
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371371
    reference: chr 6
allele count: 1
allele frequency: 9.488746346832657e-6
allele num: 105388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12145-29C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19270-29C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3136-29C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12472-29C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11494-29C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17758-29C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18736-29C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6074-29C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18403-29C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13939
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12249
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10628
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/6-56371376-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371376
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371376
    reference: chr 6
allele count: 2
allele frequency: 1.902442736473632e-5
allele num: 105128
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6074-34T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12472-34T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18403-34T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3136-34T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17758-34T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18736-34T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12145-34T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19270-34T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11494-34T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15146
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14613
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6649
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

6-56371376-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371376
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371376
    reference: chr 6
allele count: 3
allele frequency: 2.853664104710448e-5
allele num: 105128
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12145-34T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11494-34T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12472-34T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19270-34T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17758-34T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6074-34T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18403-34T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3136-34T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18736-34T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13785
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4318
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4381
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2246
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

6-56371378-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371378
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371378
    reference: chr 6
allele count: 1
allele frequency: 9.543077451616597e-6
allele num: 104788
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12472-36T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3136-36T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18403-36T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11494-36T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18736-36T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17758-36T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19270-36T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6074-36T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12145-36T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13689
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4304
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2252
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10408
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-56371380-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371380
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371380
    reference: chr 6
allele count: 1
allele frequency: 9.53397910151781e-6
allele num: 104888
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6074-38A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12472-38A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17758-38A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19270-38A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3136-38A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18736-38A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12145-38A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11494-38A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18403-38A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10352
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5596
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-56371391-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371391
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371391
    reference: chr 6
allele count: 4
allele frequency: 3.836488845408682e-5
allele num: 104262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6074-49T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18736-49T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19270-49T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17758-49T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11494-49T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18403-49T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12472-49T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12145-49T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3136-49T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11163
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2716
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

6-56371417-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371417
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371417
    reference: chr 6
allele count: 2
allele frequency: 1.749720044792833e-5
allele num: 114304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+48A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+48A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+48A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+48A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+48A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+48A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+48A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+48A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+48A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11790
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10911
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1722
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

6-56371421-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371421
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371421
    reference: chr 6
allele count: 1
allele frequency: 8.745692746322435e-6
allele num: 114342
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+44A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+44A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+44A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+44A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+44A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+44A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+44A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+44A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+44A>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7368
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3125
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/6-56371426-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371426
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371426
    reference: chr 6
allele count: 1
allele frequency: 8.719003940989781e-6
allele num: 114692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+39T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+39T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+39T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+39T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+39T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+39T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+39T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+39T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+39T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5836
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

6-56371426-ACTTTTTAAAAGCCATT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371426
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371410
    reference: chr 6
allele count: 2
allele frequency: 1.743800788197956e-5
allele num: 114692
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19792
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3302
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2269
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: ACTTTTTAAAAGCCATT
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

6-56371433-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371433
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371433
    reference: chr 6
allele count: 1
allele frequency: 8.694442512346109e-6
allele num: 115016
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+32T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+32T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+32T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+32T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+32T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+32T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+32T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+32T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+32T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2206
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7402
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

6-56371434-A-ACTAGTTAACT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371434
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371444
    reference: chr 6
allele count: 7
allele frequency: 6.079449722950791e-5
allele num: 115142
alternate allele: ACTAGTTAACT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13821
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6658
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25374
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3501
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1613
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

6-56371437-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371437
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371437
    reference: chr 6
allele count: 7
allele frequency: 6.058403004967891e-5
allele num: 115542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+28C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14155
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26866
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3617
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-56371439-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371439
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371439
    reference: chr 6
allele count: 7
allele frequency: 6.035419289200048e-5
allele num: 115982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+26G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+26G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+26G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+26G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+26G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+26G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+26G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+26G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+26G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14404
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

6-56371440-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371440
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371441
    reference: chr 6
allele count: 7
allele frequency: 6.022541512518283e-5
allele num: 116230
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+24_12471+25insC
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+24_18735+25insC
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+24_*6073+25insC
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+24_18402+25insC
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+24_12144+25insC
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+24_11493+25insC
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+24_19269+25insC
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+24_17757+25insC
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+24_3135+25insC
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6940
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14465
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7117
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-56371442-T-TAACTAAAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371442
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371451
    reference: chr 6
allele count: 7
allele frequency: 6.00817111271329e-5
allele num: 116508
alternate allele: TAACTAAAAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7017
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14565
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7188
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2189
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

6-56371444-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371444
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371444
    reference: chr 6
allele count: 1
allele frequency: 8.550224015869215e-6
allele num: 116956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+21A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+21A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+21A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+21A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+21A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+21A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+21A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+21A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+21A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29103
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-56371445-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371445
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371445
    reference: chr 6
allele count: 2
allele frequency: 1.708642312818235e-5
allele num: 117052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+20C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+20C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+20C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+20C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+20C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+20C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+20C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+20C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+20C>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

6-56371446-ATAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371446
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371442
    reference: chr 6
allele count: 3
allele frequency: 2.556585764930461e-5
allele num: 117344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+15_*6073+18delCTTA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+15_12471+18delCTTA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+15_18735+18delCTTA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+15_19269+18delCTTA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+15_18402+18delCTTA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+15_3135+18delCTTA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+15_11493+18delCTTA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+15_17757+18delCTTA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+15_12144+18delCTTA
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: ATAAG
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-56371457-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371457
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371457
    reference: chr 6
allele count: 4
allele frequency: 3.3664366268305e-5
allele num: 118820
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+8T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+8T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+8T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+8T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+8T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+8T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+8T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+8T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+8T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15289
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7566
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
hgvs: c.11493+8T>G
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP

6-56371460-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371460
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371460
    reference: chr 6
allele count: 2
allele frequency: 1.68061577762092e-5
allele num: 119004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12144+5A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17757+5A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12471+5A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18402+5A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11493+5A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19269+5A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18735+5A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6073+5A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3135+5A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26998
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15354
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 9.25e1
  variant carriers: 0
hgvs: c.11493+5A>G
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

6-56371481-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371481
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371481
    reference: chr 6
allele count: 10
allele frequency: 8.327504080477e-5
allele num: 120084
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11477A>G
  hgvsp: ENSP00000244364.6:p.Lys3826Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18719A>G
  hgvsp: ENSP00000359805.4:p.Lys6240Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3119A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18386A>G
  hgvsp: ENSP00000354508.3:p.Lys6129Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12455A>G
  hgvsp: ENSP00000400883.2:p.Lys4152Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17741A>G
  hgvsp: ENSP00000393645.2:p.Lys5914Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6057A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19253A>G
  hgvsp: ENSP00000359790.5:p.Lys6418Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12128A>G
  hgvsp: ENSP00000359824.2:p.Lys4043Arg
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2998
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys3826Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

6-56371483-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56371483
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56371483
    reference: chr 6
allele count: 75
allele frequency: 6.244276080259762e-4
allele num: 120110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.17739C>A
  hgvsp: ENST00000446842.2:c.17739C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.11475C>A
  hgvsp: ENST00000244364.6:c.11475C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.19251C>A
  hgvsp: ENST00000370754.5:c.19251C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.*6055C>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.18717C>A
  hgvsp: ENST00000370769.4:c.18717C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.12126C>A
  hgvsp: ENST00000370788.2:c.12126C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.12453C>A
  hgvsp: ENST00000421834.2:c.12453C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.18384C>A
  hgvsp: ENST00000361203.3:c.18384C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151914
  ensembl transcript: ENST00000340834
  gene symbol: DST
  hgvsc: ENST00000340834.4:n.3117C>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15576
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8019
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 3
hgvs: p.Val3825Val
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 1041
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43593
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.368615462998345e-5
allele num: 15702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.652465e6

FS
type: SiteQuality
SIO_000300: 2.112e0

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.419e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.159e1

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

BaseQRankSum
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SIO_000300: -2.079e0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532848953064165e-5
allele num: 65238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11096
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.366182836771072e-5
allele num: 15708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.08e-1

FS
type: SiteQuality
SIO_000300: 6.936e0

ClippingRankSum
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SIO_000300: -7.57e-1

QD
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MQRankSum
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SIO_000300: -3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.653585e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532332209623046e-5
allele num: 65260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
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MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
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ReadPosRankSum
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SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 1.0638e1

BaseQRankSum
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QD
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SIO_000300: 1.351e1

MQ
type: SiteQuality
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VQSLOD
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SIO_000300: -1.392e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15740
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.004141905276428e-5
allele num: 11106
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.654417e6

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

QD
type: SiteQuality
SIO_000300: 1.039e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 285
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533036946190403e-5
allele num: 65230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11098
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15746
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.26e-1

FS
type: SiteQuality
SIO_000300: 1.694e0

DP
type: SiteQuality
SIO_000300: 1.653358e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.042e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

QD
type: SiteQuality
SIO_000300: 1.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e-1

GenotypeQuality
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variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11076
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 1
allele frequency: 6.36213258684311e-5
allele num: 15718
num of homozygotes: 0

African
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

MQRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
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SIO_000300: 1.151e1

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65104
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8486
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11066
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South Asian
type: Population
allele count: 1
allele frequency: 6.369426751592356e-5
allele num: 15700
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.48e-1

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.649664e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.536759282026063e-5
allele num: 65072
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 8.494999999999999e0

DP
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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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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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9480
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 7.270964614638875e-4
allele num: 8252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15286
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.931e0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.42e-1

QD
type: SiteQuality
SIO_000300: 1.233e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 1.597958e6

GenotypeQuality
all individuals: 993
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.171884416531862e-5
allele num: 63054
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15208
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.031e1

MQRankSum
type: SiteQuality
SIO_000300: -6.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 9.28e-1

DP
type: SiteQuality
SIO_000300: 1.587556e6

VQSLOD
type: SiteQuality
SIO_000300: 5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10646
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.060670343657191e-4
allele num: 9428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62934
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15176
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

MQ
type: SiteQuality
SIO_000300: 5.914e1

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-2

FS
type: SiteQuality
SIO_000300: 7.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.112e0

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

DP
type: SiteQuality
SIO_000300: 1.582891e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 616
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variant carriers: 0

GenotypeQuality
all individuals: 2092
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.2531328320802e-4
allele num: 7980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14950
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61622
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.379e1

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.323e0

DP
type: SiteQuality
SIO_000300: 1.523052e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.800870511425463e-5
allele num: 14704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

DP
type: SiteQuality
SIO_000300: 1.461295e6

VQSLOD
type: SiteQuality
SIO_000300: -3.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

FS
type: SiteQuality
SIO_000300: 1.2457e1

QD
type: SiteQuality
SIO_000300: 6.09e0

MQ
type: SiteQuality
SIO_000300: 5.014e1

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14666
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.287001287001287e-4
allele num: 7770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9148
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60266
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.033e1

DP
type: SiteQuality
SIO_000300: 1.45303e6

FS
type: SiteQuality
SIO_000300: 1.785e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12123
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9906
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7752
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.839945280437756e-5
allele num: 14620
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.63e-1

FS
type: SiteQuality
SIO_000300: 6.335e0

VQSLOD
type: SiteQuality
SIO_000300: -1.599e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 5.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.41e0

DP
type: SiteQuality
SIO_000300: 1.445003e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5021
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 966
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 3.017703862660944e-4
allele num: 59648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9074
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.506180871828237e-4
allele num: 6148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14582
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.349e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

MQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 965
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GenotypeQuality
all individuals: 637
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.436255652291287e-5
allele num: 59268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9024
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

QD
type: SiteQuality
SIO_000300: 8.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

DP
type: SiteQuality
SIO_000300: 1.386222e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.75e-1

GenotypeQuality
all individuals: 538
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19465
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9010
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14474
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.029866117404737e-4
allele num: 9710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.183672089012141e-4
allele num: 59138
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.258e1

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.276e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

DP
type: SiteQuality
SIO_000300: 1.385083e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.755371436595984e-5
allele num: 56968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

VQSLOD
type: SiteQuality
SIO_000300: 9.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e0

FS
type: SiteQuality
SIO_000300: 1.427e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.279963e6

QD
type: SiteQuality
SIO_000300: 1.664e1

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.774622892635315e-4
allele num: 56350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9060
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13960
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.267215e6

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

QD
type: SiteQuality
SIO_000300: 1.416e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 820
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variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13928
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.784758165268606e-5
allele num: 56030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.264336e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

MQRankSum
type: SiteQuality
SIO_000300: 7.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.167e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8860
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7018
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13824
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.54e1

DP
type: SiteQuality
SIO_000300: 1.261106e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQ
type: SiteQuality
SIO_000300: 5.874e1

VQSLOD
type: SiteQuality
SIO_000300: -7.993e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6892
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.825950407186941e-5
allele num: 54766
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

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

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

MQ
type: SiteQuality
SIO_000300: 5.889e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53398
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5776
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.483899688381065e-4
allele num: 13478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6648
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.25454e6

MQ
type: SiteQuality
SIO_000300: 5.877e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.023e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5651
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.467308166790032e-5
allele num: 40530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4650
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.466275659824047e-4
allele num: 6820
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.189060642092747e-4
allele num: 8410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5338
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.51e0

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

DP
type: SiteQuality
SIO_000300: 1.031267e6

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
all individuals: 5880
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 137
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4936
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.459427904261529e-4
allele num: 6852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4664
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.625346901017577e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40840
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.037629e6

MQRankSum
type: SiteQuality
SIO_000300: -1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

FS
type: SiteQuality
SIO_000300: 1.3134e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.468e0

QD
type: SiteQuality
SIO_000300: 1.499e1

GenotypeQuality
all individuals: 5656
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 372
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5006
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.422715379397228e-5
allele num: 41276
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4700
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.768e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.9e-3

QD
type: SiteQuality
SIO_000300: 4.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.072e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.036e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.049385e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 579
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 331
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.243963737546001e-5
allele num: 44564
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

DP
type: SiteQuality
SIO_000300: 1.165351e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.08e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

FS
type: SiteQuality
SIO_000300: 4.421e0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 441
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 211
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variant carriers: 1

GenotypeQuality
all individuals: 511
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.468360111300602e-4
allele num: 44564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5580
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 1.165351e6

FS
type: SiteQuality
SIO_000300: 4.421e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

QD
type: SiteQuality
SIO_000300: 1.29e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 431
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GenotypeQuality
all individuals: 217
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.198092056095309e-5
allele num: 45494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4950
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5718
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.188293e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

QD
type: SiteQuality
SIO_000300: 1.057e1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-2

MQ
type: SiteQuality
SIO_000300: 5.914e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.286e0

GenotypeQuality
all individuals: 5799
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
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GenotypeQuality
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GenotypeQuality
all individuals: 1027
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GenotypeQuality
all individuals: 4776
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1421
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.38365772400491e-5
allele num: 45624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5748
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

DP
type: SiteQuality
SIO_000300: 1.198528e6

FS
type: SiteQuality
SIO_000300: 7.947e0

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

QD
type: SiteQuality
SIO_000300: 5.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

VQSLOD
type: SiteQuality
SIO_000300: -5.639e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 870
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 221
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5044
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.688048615800135e-4
allele num: 5924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.091e0

DP
type: SiteQuality
SIO_000300: 1.22031e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

QD
type: SiteQuality
SIO_000300: 1.246e1

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: 7

GenotypeQuality
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GenotypeQuality
all individuals: 693
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.177658142664872e-3
allele num: 5944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47024
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
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European (Finnish)
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: 642
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

FS
type: SiteQuality
SIO_000300: 6.119e0

MQRankSum
type: SiteQuality
SIO_000300: -1.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.44e1

DP
type: SiteQuality
SIO_000300: 1.230883e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 157
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GenotypeQuality
all individuals: 528
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GenotypeQuality
all individuals: 840
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.109170674090947e-5
allele num: 47412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.039e0

MQRankSum
type: SiteQuality
SIO_000300: -7.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.355e0

DP
type: SiteQuality
SIO_000300: 1.237517e6

QD
type: SiteQuality
SIO_000300: 1.197e1

GenotypeQuality
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bin: 7.5e0
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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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.286670097786928e-4
allele num: 7772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.038819115968031e-5
allele num: 49048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7212
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.428e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

DP
type: SiteQuality
SIO_000300: 1.279052e6

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

QD
type: SiteQuality
SIO_000300: 1.433e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.4530853761623e-5
allele num: 11830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8302
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53984
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

DP
type: SiteQuality
SIO_000300: 1.392558e6

VQSLOD
type: SiteQuality
SIO_000300: -1.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.646e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14052
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.622217896307832e-5
allele num: 61644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9076
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.129999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.561616e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.197e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.483e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 600
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variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.245019920318725e-4
allele num: 8032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62010
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

DP
type: SiteQuality
SIO_000300: 1.568254e6

FS
type: SiteQuality
SIO_000300: 6.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 8.970000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.3e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 268
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.609943008017516e-5
allele num: 62114
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8044
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.321e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

QD
type: SiteQuality
SIO_000300: 1.112e1

DP
type: SiteQuality
SIO_000300: 1.571337e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.762e0

MQ
type: SiteQuality
SIO_000300: 5.782e1

FS
type: SiteQuality
SIO_000300: 1.233e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.476e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62638
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.531071292413267e-5
allele num: 10492
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14492
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.29e-1

VQSLOD
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.94e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10582
num of homozygotes: 0

Other
type: Population
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: 6372
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63058
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African
type: Population
allele count: 1
allele frequency: 1.079680414597279e-4
allele num: 9262
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.808e1

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

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -4.608e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.730380939561179e-5
allele num: 14858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63104
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10620
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

MQRankSum
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DP
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: 7.66e-1

InbreedingCoeff
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SIO_000300: 1.2e-3

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -7.66e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 6.17e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.722237160527024e-5
allele num: 14876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.58609313538891e-5
allele num: 63048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.59e-1

QD
type: SiteQuality
SIO_000300: 9.42e0

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 5.620000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

DP
type: SiteQuality
SIO_000300: 1.589694e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.591343093570974e-5
allele num: 62840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.575741e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.393051031487514e-5
allele num: 58944
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.784e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

MQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

DP
type: SiteQuality
SIO_000300: 1.371453e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.31e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9664
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.393051031487514e-5
allele num: 58944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14760
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 1.784e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.31e-1

DP
type: SiteQuality
SIO_000300: 1.371453e6

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.719749604457591e-5
allele num: 58148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7118
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.347551e6

MQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.524e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.69e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7100
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58056
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14772
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.12943302462164e-4
allele num: 8854
num of homozygotes: 0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
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SIO_000300: -2.468e0

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.777e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.346576e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7078
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.459010722933241e-5
allele num: 57820
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.344175e6

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

QD
type: SiteQuality
SIO_000300: 1.265e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7078
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9516
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.030044660982542e-4
allele num: 14778
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57820
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.314e0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14766
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.129688206055129e-4
allele num: 8852
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.18e-2

FS
type: SiteQuality
SIO_000300: 7.102e0

QD
type: SiteQuality
SIO_000300: 1.885e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

DP
type: SiteQuality
SIO_000300: 1.343892e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14782
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.734304543877905e-5
allele num: 57660
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7056
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6248
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: -5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.197e0

DP
type: SiteQuality
SIO_000300: 1.343821e6

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.199e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57174
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.697963037906381e-4
allele num: 14826
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

DP
type: SiteQuality
SIO_000300: 1.359051e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.127000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

QD
type: SiteQuality
SIO_000300: 1.318e1

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: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.192746080904186e-5
allele num: 62642
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.700227e6

MQRankSum
type: SiteQuality
SIO_000300: -2.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e0

VQSLOD
type: SiteQuality
SIO_000300: -2.457e0

FS
type: SiteQuality
SIO_000300: 1.8647e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

QD
type: SiteQuality
SIO_000300: 1.384e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.594896331738437e-5
allele num: 62700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16160
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.443e0

QD
type: SiteQuality
SIO_000300: 7.48e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 1.717319e6

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62904
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.177415369409439e-5
allele num: 16188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10862
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.742954e6

MQ
type: SiteQuality
SIO_000300: 5.552e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.319e0

MQRankSum
type: SiteQuality
SIO_000300: -2.676e0

FS
type: SiteQuality
SIO_000300: 3.049e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

QD
type: SiteQuality
SIO_000300: 1.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: -5.238e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9520
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.538071065989848e-4
allele num: 7880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.049e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.319e0

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.742954e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.58473582453805e-5
allele num: 63102
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.786273e6

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 2.2e-2

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63160
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 8.822788001008318e-4
allele num: 7934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63410
num of homozygotes: 0

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

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

East Asian
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allele frequency: 8.76533934385174e-4
allele num: 7986
num of homozygotes: 0

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

MQRankSum
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SIO_000300: -3.413e0

FS
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BaseQRankSum
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VQSLOD
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QD
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DP
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MQ
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

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

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

East Asian
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allele count: 7
allele frequency: 8.697813121272366e-4
allele num: 8048
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11024
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63690
num of homozygotes: 0

BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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QD
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63846
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

East Asian
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allele count: 7
allele frequency: 8.684863523573201e-4
allele num: 8060
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.257e1

DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11084
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: 16300
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64008
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

East Asian
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allele count: 7
allele frequency: 8.639842014317452e-4
allele num: 8102
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 6.67e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.257e1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

DP
type: SiteQuality
SIO_000300: 1.845015e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

VQSLOD
type: SiteQuality
SIO_000300: 5.42e-1

GenotypeQuality
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variant carriers: 1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555451858764971e-5
allele num: 64290
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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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: 6526
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.66e-2

MQ
type: SiteQuality
SIO_000300: 5.983e1

DP
type: SiteQuality
SIO_000300: 1.854807e6

MQRankSum
type: SiteQuality
SIO_000300: 9.85e-1

VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.02e-1

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

Other
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allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.106265337185102e-5
allele num: 64386
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African
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Latino
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InbreedingCoeff
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MQ
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 64550
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South Asian
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Latino
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allele frequency: 1.790830945558739e-4
allele num: 11168
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European (Finnish)
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East Asian
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MQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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FS
type: SiteQuality
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DP
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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allele num: 65528
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Latino
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African
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Other
type: Population
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European (Finnish)
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East Asian
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ClippingRankSum
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QD
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FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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allele frequency: 6.082725060827251e-5
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Latino
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Other
type: Population
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European (Non-Finnish)
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European (Finnish)
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East Asian
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allele num: 8420
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ReadPosRankSum
type: SiteQuality
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DP
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ClippingRankSum
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MQ
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BaseQRankSum
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FS
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MQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 7.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3136
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7640
bin: 9.75e1
variant carriers: 10

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

GenotypeQuality
all individuals: 7796
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4243
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30798
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.50684105840516e-4
allele num: 66364
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.41e-1

QD
type: SiteQuality
SIO_000300: 1.383e1

DP
type: SiteQuality
SIO_000300: 1.912916e6