6-56480674-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480674
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480674
    reference: chr 6
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7591A>G
  hgvsp: ENSP00000359801.6:p.Ile2531Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1392A>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.4831-1392A>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.3319-1392A>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.3319-1392A>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.4297-1392A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1392A>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.4297-1392A>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.4297-1392A>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.4297-1392A>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.4297-1392A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile2531Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/6-56480684-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480684
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480684
    reference: chr 6
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7581T>G
  hgvsp: ENSP00000359801.6:p.Ile2527Met
  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.3319-1402T>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.4297-1402T>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.3319-1402T>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.4297-1402T>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.4297-1402T>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.4831-1402T>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.4297-1402T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1402T>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.4297-1402T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1402T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile2527Met
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD

6-56480685-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480685
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480685
    reference: chr 6
allele count: 6
allele frequency: 4.943723942455053e-5
allele num: 121366
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.4297-1403T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7580T>C
  hgvsp: ENSP00000359801.6:p.Ile2527Thr
  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.4297-1403T>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.4297-1403T>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.3319-1403T>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.4297-1403T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1403T>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.4831-1403T>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.3319-1403T>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.4297-1403T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1403T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10414
  bin: 9.75e1
  variant carriers: 6
hgvs: p.Ile2527Thr
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-56480687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480687
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480687
    reference: chr 6
allele count: 15
allele frequency: 1.235849522962084e-4
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.4297-1405G>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.4831-1405G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1405G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7578G>A
  hgvsp: ENST00000370765.6:c.7578G>A(p.%3D)
  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.3319-1405G>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.4297-1405G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1405G>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.4297-1405G>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.3319-1405G>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.4297-1405G>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.4297-1405G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly2526Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

6-56480690-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480690
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480690
    reference: chr 6
allele count: 2
allele frequency: 1.647799363949445e-5
allele num: 121374
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.4297-1408A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1408A>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.4297-1408A>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.4297-1408A>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.3319-1408A>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.4831-1408A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7575A>G
  hgvsp: ENST00000370765.6:c.7575A>G(p.%3D)
  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.4297-1408A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1408A>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.4297-1408A>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.3319-1408A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr2525Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP

6-56480691-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480691
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480691
    reference: chr 6
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.4297-1409C>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.3319-1409C>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.4297-1409C>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.4297-1409C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1409C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7574C>G
  hgvsp: ENSP00000359801.6:p.Thr2525Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1409C>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.4831-1409C>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.4297-1409C>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.3319-1409C>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.4297-1409C>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr2525Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

6-56480699-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480699
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480699
    reference: chr 6
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
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.4297-1417A>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.4297-1417A>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.3319-1417A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1417A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1417A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7566A>G
  hgvsp: ENST00000370765.6:c.7566A>G(p.%3D)
  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.4831-1417A>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.3319-1417A>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.4297-1417A>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.4297-1417A>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.4297-1417A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu2522Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

6-56480708-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480708
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480708
    reference: chr 6
allele count: 10
allele frequency: 8.239675686364985e-5
allele num: 121364
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.4297-1426G>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.4297-1426G>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.4297-1426G>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.3319-1426G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1426G>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.3319-1426G>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.4297-1426G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7557G>A
  hgvsp: ENST00000370765.6:c.7557G>A(p.%3D)
  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.4297-1426G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1426G>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.4831-1426G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln2519Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

6-56480712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480712
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480712
    reference: chr 6
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.4297-1430G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7553G>A
  hgvsp: ENSP00000359801.6:p.Arg2518Gln
  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.3319-1430G>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.4297-1430G>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.4831-1430G>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.3319-1430G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1430G>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.4297-1430G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1430G>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.4297-1430G>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.4297-1430G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg2518Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum

6-56480713-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480713
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480713
    reference: chr 6
allele count: 6
allele frequency: 4.944375772558714e-5
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7552C>T
  hgvsp: ENSP00000359801.6:p.Arg2518Ter
  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.4297-1431C>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.4297-1431C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1431C>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.3319-1431C>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.4297-1431C>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.3319-1431C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1431C>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.4297-1431C>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.4831-1431C>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.4297-1431C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg2518Ter
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-56480714-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480714
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480714
    reference: chr 6
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
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.4297-1432G>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.4831-1432G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1432G>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.3319-1432G>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.4297-1432G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7551G>A
  hgvsp: ENST00000370765.6:c.7551G>A(p.%3D)
  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.4297-1432G>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.4297-1432G>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.3319-1432G>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.4297-1432G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1432G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3903
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu2517Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

6-56480720-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480720
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480721
    reference: chr 6
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.4297-1439dupA
  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.3319-1439dupA
  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.3319-1439dupA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1439dupA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1439dupA
  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.4297-1439dupA
  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.4297-1439dupA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7544dupA
  hgvsp: ENSP00000359801.6:p.Gln2516AlafsTer6
  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.4297-1439dupA
  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.4831-1439dupA
  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.4297-1439dupA
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln2516AlafsTer6
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

6-56480730-C-CTTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480730
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480733
    reference: chr 6
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: CTTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.4297-1449_4297-1448insAAA
  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.4297-1449_4297-1448insAAA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7534_7535insAAA
  hgvsp: ENSP00000359801.6:p.Gly2512delinsGluArg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1449_4417-1448insAAA
  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.3319-1449_3319-1448insAAA
  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.4297-1449_4297-1448insAAA
  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.3319-1449_3319-1448insAAA
  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.4297-1449_4297-1448insAAA
  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.4297-1449_4297-1448insAAA
  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.4831-1449_4831-1448insAAA
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1449_3319-1448insAAA
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: protein altering
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly2512delinsGluArg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

6-56480731-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480731
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480731
    reference: chr 6
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
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.4297-1449G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1449G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7534G>C
  hgvsp: ENSP00000359801.6:p.Gly2512Arg
  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.3319-1449G>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.4297-1449G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1449G>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.4297-1449G>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.4297-1449G>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.3319-1449G>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.4297-1449G>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.4831-1449G>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly2512Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

6-56480731-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480731
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480731
    reference: chr 6
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7534G>A
  hgvsp: ENSP00000359801.6:p.Gly2512Arg
  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.4297-1449G>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.4831-1449G>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.4297-1449G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1449G>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.4297-1449G>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.4297-1449G>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.3319-1449G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1449G>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.3319-1449G>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.4297-1449G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly2512Arg
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/6-56480735-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480735
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480735
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
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.3319-1453T>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.4297-1453T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1453T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7530T>G
  hgvsp: ENSP00000359801.6:p.Asp2510Glu
  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.4297-1453T>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.3319-1453T>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.4297-1453T>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.4297-1453T>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.4831-1453T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1453T>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.4297-1453T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp2510Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

6-56480744-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480744
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480744
    reference: chr 6
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
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.4297-1462C>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.4297-1462C>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.3319-1462C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7521C>T
  hgvsp: ENST00000370765.6:c.7521C>T(p.%3D)
  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.3319-1462C>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.4297-1462C>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.4297-1462C>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.4297-1462C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1462C>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.4831-1462C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1462C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10414
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly2507Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-56480744-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480744
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480744
    reference: chr 6
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
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.4297-1462C>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.4297-1462C>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.3319-1462C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7521C>G
  hgvsp: ENST00000370765.6:c.7521C>G(p.%3D)
  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.4297-1462C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1462C>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.4831-1462C>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.4297-1462C>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.3319-1462C>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.4297-1462C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1462C>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly2507Gly
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

6-56480745-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480745
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480745
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
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.4297-1463G>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.3319-1463G>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.4297-1463G>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.3319-1463G>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.4297-1463G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1463G>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.4297-1463G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7520G>C
  hgvsp: ENSP00000359801.6:p.Gly2507Ala
  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.4831-1463G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1463G>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.4297-1463G>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly2507Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

6-56480752-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480752
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480752
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
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.4831-1470C>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.3319-1470C>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.4297-1470C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7513C>T
  hgvsp: ENSP00000359801.6:p.His2505Tyr
  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.4297-1470C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1470C>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.3319-1470C>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.4297-1470C>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.4297-1470C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1470C>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.4297-1470C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His2505Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

6-56480761-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480761
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480761
    reference: chr 6
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.4297-1479G>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.4297-1479G>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.3319-1479G>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.4831-1479G>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.4297-1479G>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.4297-1479G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1479G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7504G>A
  hgvsp: ENSP00000359801.6:p.Glu2502Lys
  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.3319-1479G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1479G>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.4297-1479G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu2502Lys
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

6-56480762-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480762
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480762
    reference: chr 6
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
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.4297-1480C>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.4831-1480C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7503C>T
  hgvsp: ENST00000370765.6:c.7503C>T(p.%3D)
  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.4297-1480C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1480C>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.4297-1480C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1480C>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.3319-1480C>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.3319-1480C>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.4297-1480C>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.4297-1480C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala2501Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-56480769-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480769
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480769
    reference: chr 6
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
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.4297-1487G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1487G>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.4297-1487G>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.4831-1487G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7496G>T
  hgvsp: ENSP00000359801.6:p.Arg2499Leu
  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.3319-1487G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1487G>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.4297-1487G>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.3319-1487G>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.4297-1487G>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.4297-1487G>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3892
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg2499Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

6-56480769-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480769
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480769
    reference: chr 6
allele count: 3
allele frequency: 2.472636159831201e-5
allele num: 121328
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.3319-1487G>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.4297-1487G>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.4831-1487G>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.4297-1487G>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.3319-1487G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7496G>A
  hgvsp: ENSP00000359801.6:p.Arg2499Gln
  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.4297-1487G>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.4297-1487G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1487G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1487G>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.4297-1487G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg2499Gln
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

6-56480770-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480770
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480770
    reference: chr 6
allele count: 6
allele frequency: 4.945516888940176e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7495C>T
  hgvsp: ENSP00000359801.6:p.Arg2499Trp
  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.3319-1488C>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.4297-1488C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1488C>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.4831-1488C>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.4297-1488C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1488C>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.4297-1488C>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.4297-1488C>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.3319-1488C>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.4297-1488C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg2499Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-56480774-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480774
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480774
    reference: chr 6
allele count: 185
allele frequency: 1.524867707423221e-3
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.4297-1492G>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.4297-1492G>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.3319-1492G>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.3319-1492G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7491G>A
  hgvsp: ENST00000370765.6:c.7491G>A(p.%3D)
  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.4831-1492G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1492G>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.4297-1492G>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.4297-1492G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1492G>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.4297-1492G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 9.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 10146
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 20490
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17313
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys2497Lys
num of homozygotes: 2
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-56480775-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480775
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480775
    reference: chr 6
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
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.4297-1493A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1493A>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.4297-1493A>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.4297-1493A>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.3319-1493A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1493A>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.4297-1493A>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.4297-1493A>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.4831-1493A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7490A>G
  hgvsp: ENSP00000359801.6:p.Lys2497Arg
  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.3319-1493A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys2497Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

6-56480777-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480777
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480777
    reference: chr 6
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4831-1495A>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.4297-1495A>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.3319-1495A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1495A>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.4297-1495A>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.4297-1495A>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.3319-1495A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7488A>C
  hgvsp: ENSP00000359801.6:p.Lys2496Asn
  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.4297-1495A>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.4297-1495A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1495A>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys2496Asn
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

6-56480788-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480788
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480788
    reference: chr 6
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.4297-1506C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7477C>G
  hgvsp: ENSP00000359801.6:p.Leu2493Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1506C>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.4297-1506C>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.3319-1506C>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.4297-1506C>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.3319-1506C>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.4831-1506C>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.4297-1506C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1506C>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.4297-1506C>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8213
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu2493Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

6-56480791-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480791
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480791
    reference: chr 6
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1509C>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.4831-1509C>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.4297-1509C>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.3319-1509C>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.4297-1509C>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.3319-1509C>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.4297-1509C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1509C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7474C>T
  hgvsp: ENSP00000359801.6:p.Pro2492Ser
  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.4297-1509C>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.4297-1509C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro2492Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

6-56480794-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480794
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480794
    reference: chr 6
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
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.4297-1512G>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.3319-1512G>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.4831-1512G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7471G>C
  hgvsp: ENSP00000359801.6:p.Asp2491His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1512G>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.4297-1512G>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.3319-1512G>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.4297-1512G>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.4297-1512G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1512G>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.4297-1512G>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp2491His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

6-56480801-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480801
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480801
    reference: chr 6
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
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.4831-1519C>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.3319-1519C>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.4297-1519C>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.4297-1519C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1519C>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.3319-1519C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7464C>T
  hgvsp: ENST00000370765.6:c.7464C>T(p.%3D)
  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.4297-1519C>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.4297-1519C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1519C>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.4297-1519C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly2488Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

6-56480811-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480811
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480811
    reference: chr 6
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7454G>A
  hgvsp: ENSP00000359801.6:p.Ser2485Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1529G>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.4297-1529G>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.4297-1529G>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.4297-1529G>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.3319-1529G>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.4297-1529G>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.3319-1529G>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.4831-1529G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1529G>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.4297-1529G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser2485Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

6-56480813-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480813
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480813
    reference: chr 6
allele count: 2
allele frequency: 1.648641519388024e-5
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.4297-1531C>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.3319-1531C>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.4297-1531C>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.3319-1531C>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.4831-1531C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1531C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7452C>T
  hgvsp: ENST00000370765.6:c.7452C>T(p.%3D)
  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.4297-1531C>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.4297-1531C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1531C>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.4297-1531C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val2484Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

6-56480816-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480816
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480816
    reference: chr 6
allele count: 4
allele frequency: 3.297717979158422e-5
allele num: 121296
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.3319-1534A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7449A>G
  hgvsp: ENST00000370765.6:c.7449A>G(p.%3D)
  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.4297-1534A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1534A>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.4297-1534A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1534A>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.3319-1534A>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.4297-1534A>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.4297-1534A>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.4831-1534A>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.4297-1534A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10487
  bin: 9.75e1
  variant carriers: 4
hgvs: p.Gln2483Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-56480819-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480819
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480819
    reference: chr 6
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7446C>A
  hgvsp: ENST00000370765.6:c.7446C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1537C>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.3319-1537C>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.4297-1537C>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.4297-1537C>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1537C>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.3319-1537C>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.4297-1537C>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.4297-1537C>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.4831-1537C>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.4297-1537C>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala2482Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

6-56480825-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480825
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480825
    reference: chr 6
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
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.4297-1543T>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.4297-1543T>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.4831-1543T>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.3319-1543T>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.3319-1543T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1543T>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.4297-1543T>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.4297-1543T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7440T>C
  hgvsp: ENST00000370765.6:c.7440T>C(p.%3D)
  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.4297-1543T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1543T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8193
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu2480Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-56480826-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480826
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480826
    reference: chr 6
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4831-1544T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1544T>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.3319-1544T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7439T>C
  hgvsp: ENSP00000359801.6:p.Leu2480Pro
  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.4297-1544T>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.4297-1544T>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.4297-1544T>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.4297-1544T>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.3319-1544T>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.4297-1544T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1544T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3878
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu2480Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

6-56480832-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480832
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480832
    reference: chr 6
allele count: 3
allele frequency: 2.473166147301776e-5
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1550G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7433G>A
  hgvsp: ENSP00000359801.6:p.Arg2478Gln
  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.3319-1550G>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.3319-1550G>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.4297-1550G>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.4297-1550G>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.4831-1550G>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.4297-1550G>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.4297-1550G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1550G>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.4297-1550G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg2478Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

6-56480833-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480833
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480833
    reference: chr 6
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.4297-1551C>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.4297-1551C>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.4831-1551C>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.3319-1551C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7432C>T
  hgvsp: ENSP00000359801.6:p.Arg2478Ter
  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.4297-1551C>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.4297-1551C>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.4297-1551C>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.3319-1551C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1551C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1551C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg2478Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

6-56480847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480847
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480847
    reference: chr 6
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.4297-1565G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1565G>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.4831-1565G>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.4297-1565G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7418G>A
  hgvsp: ENSP00000359801.6:p.Arg2473Gln
  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.3319-1565G>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.4297-1565G>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.3319-1565G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1565G>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.4297-1565G>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.4297-1565G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3981
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg2473Gln
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

6-56480848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480848
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480848
    reference: chr 6
allele count: 3
allele frequency: 2.473043822336532e-5
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7417C>T
  hgvsp: ENSP00000359801.6:p.Arg2473Trp
  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.4831-1566C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1566C>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.4297-1566C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1566C>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.4297-1566C>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.3319-1566C>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.4297-1566C>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.4297-1566C>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.3319-1566C>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.4297-1566C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg2473Trp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-56480857-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480857
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480858
    reference: chr 6
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7407_7408insC
  hgvsp: ENSP00000359801.6:p.Val2471GlyfsTer2
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1576_4417-1575insC
  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.4297-1576_4297-1575insC
  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.4297-1576_4297-1575insC
  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.3319-1576_3319-1575insC
  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.4297-1576_4297-1575insC
  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.4831-1576_4831-1575insC
  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.4297-1576_4297-1575insC
  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.3319-1576_3319-1575insC
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1576_3319-1575insC
  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.4297-1576_4297-1575insC
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10074
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val2471GlyfsTer2
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

6-56480865-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480865
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480865
    reference: chr 6
allele count: 5
allele frequency: 4.12275928033114e-5
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1583G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1583G>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.4297-1583G>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.4831-1583G>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.3319-1583G>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.4297-1583G>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.4297-1583G>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.3319-1583G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7400G>A
  hgvsp: ENSP00000359801.6:p.Arg2467His
  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.4297-1583G>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.4297-1583G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg2467His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

6-56480866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480866
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480866
    reference: chr 6
allele count: 4
allele frequency: 3.298425002061515e-5
allele num: 121270
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.4297-1584C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7399C>T
  hgvsp: ENSP00000359801.6:p.Arg2467Cys
  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.4297-1584C>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.4831-1584C>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.3319-1584C>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.3319-1584C>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.4297-1584C>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.4297-1584C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1584C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1584C>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.4297-1584C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg2467Cys
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

6-56480868-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480868
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480868
    reference: chr 6
allele count: 2
allele frequency: 1.648614339647526e-5
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.4297-1586C>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.4297-1586C>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.4831-1586C>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.3319-1586C>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1586C>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7397C>A
  hgvsp: ENSP00000359801.6:p.Ser2466Tyr
  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.3319-1586C>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.4297-1586C>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.4297-1586C>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.4297-1586C>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1586C>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser2466Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

6-56480869-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480869
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480869
    reference: chr 6
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
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.4297-1587T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7396T>C
  hgvsp: ENSP00000359801.6:p.Ser2466Pro
  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.4297-1587T>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.3319-1587T>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.4297-1587T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1587T>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.4297-1587T>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.4831-1587T>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.3319-1587T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1587T>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.4297-1587T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser2466Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

6-56480876-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480876
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480876
    reference: chr 6
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1594A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7389A>G
  hgvsp: ENST00000370765.6:c.7389A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1594A>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.4297-1594A>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.4297-1594A>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.3319-1594A>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.4831-1594A>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.4297-1594A>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.3319-1594A>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.4297-1594A>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.4297-1594A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu2463Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: T
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

6-56480879-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480879
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480879
    reference: chr 6
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
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.3319-1597A>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.4297-1597A>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.4297-1597A>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.4297-1597A>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.4297-1597A>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1597A>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.3319-1597A>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7386A>T
  hgvsp: ENST00000370765.6:c.7386A>T(p.%3D)
  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.4831-1597A>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1597A>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.4297-1597A>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3982
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val2462Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-56480884-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480884
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480884
    reference: chr 6
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
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.4297-1602T>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.3319-1602T>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.4831-1602T>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.4297-1602T>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.4297-1602T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7381T>C
  hgvsp: ENSP00000359801.6:p.Ser2461Pro
  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.4297-1602T>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.3319-1602T>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.4297-1602T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1602T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1602T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24578
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser2461Pro
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

6-56480906-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480906
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480906
    reference: chr 6
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1624G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7359G>A
  hgvsp: ENST00000370765.6:c.7359G>A(p.%3D)
  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.3319-1624G>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.4297-1624G>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.3319-1624G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1624G>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.4297-1624G>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.4297-1624G>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.4297-1624G>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.4831-1624G>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.4297-1624G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu2453Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/6-56480915-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480915
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480915
    reference: chr 6
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.4297-1633G>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.4297-1633G>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.4831-1633G>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.3319-1633G>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.4297-1633G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7350G>T
  hgvsp: ENST00000370765.6:c.7350G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1633G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1633G>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.3319-1633G>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.4297-1633G>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.4297-1633G>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly2450Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

6-56480915-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480915
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480915
    reference: chr 6
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.4297-1633G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1633G>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.3319-1633G>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.4297-1633G>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.3319-1633G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7350G>A
  hgvsp: ENST00000370765.6:c.7350G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1633G>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.4297-1633G>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.4831-1633G>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.4297-1633G>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.4297-1633G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3881
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly2450Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

6-56480916-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480916
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480916
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.3319-1634G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7349G>A
  hgvsp: ENSP00000359801.6:p.Gly2450Glu
  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.4297-1634G>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.4297-1634G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1634G>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.4297-1634G>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.3319-1634G>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.4297-1634G>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.4831-1634G>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.4297-1634G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1634G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5044
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly2450Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

6-56480918-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480918
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480918
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4831-1636A>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.4297-1636A>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.4297-1636A>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.4297-1636A>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.4297-1636A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7347A>C
  hgvsp: ENST00000370765.6:c.7347A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1636A>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.4297-1636A>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.3319-1636A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1636A>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.3319-1636A>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala2449Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum

http://identifiers.org/exac.variant/6-56480921-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480921
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480921
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.3319-1639T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1639T>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.4297-1639T>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.4297-1639T>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.3319-1639T>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.4297-1639T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7344T>G
  hgvsp: ENST00000370765.6:c.7344T>G(p.%3D)
  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.4297-1639T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1639T>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.4297-1639T>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.4831-1639T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val2448Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-56480935-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480935
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480935
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7330T>G
  hgvsp: ENSP00000359801.6:p.Leu2444Val
  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.4831-1653T>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.3319-1653T>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.4297-1653T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1653T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1653T>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.4297-1653T>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.3319-1653T>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.4297-1653T>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.4297-1653T>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.4297-1653T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu2444Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-56480942-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480942
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480942
    reference: chr 6
allele count: 3
allele frequency: 2.472147142197904e-5
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.4297-1660G>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.3319-1660G>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.4297-1660G>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.4297-1660G>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.4831-1660G>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.4297-1660G>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.3319-1660G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7323G>A
  hgvsp: ENST00000370765.6:c.7323G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1660G>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.4297-1660G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1660G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3982
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys2441Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

6-56480954-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480954
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480954
    reference: chr 6
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
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.4297-1672G>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.3319-1672G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7311G>C
  hgvsp: ENST00000370765.6:c.7311G>C(p.%3D)
  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.3319-1672G>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.4831-1672G>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.4297-1672G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1672G>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.4297-1672G>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.4297-1672G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1672G>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.4297-1672G>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg2437Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

6-56480954-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480954
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480954
    reference: chr 6
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
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.4297-1672G>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.3319-1672G>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.4297-1672G>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.4297-1672G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7311G>A
  hgvsp: ENST00000370765.6:c.7311G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1672G>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.4831-1672G>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.3319-1672G>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.4297-1672G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1672G>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.4297-1672G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg2437Arg
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

6-56480955-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480955
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480955
    reference: chr 6
allele count: 2
allele frequency: 1.648016612007449e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7310G>A
  hgvsp: ENSP00000359801.6:p.Arg2437Gln
  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.4297-1673G>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.4297-1673G>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.4297-1673G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1673G>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.3319-1673G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1673G>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.3319-1673G>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.4297-1673G>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.4831-1673G>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.4297-1673G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg2437Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-56480956-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480956
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480956
    reference: chr 6
allele count: 3
allele frequency: 2.472065658063878e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1674C>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.4297-1674C>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.4297-1674C>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.4831-1674C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1674C>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.4297-1674C>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.4297-1674C>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.4297-1674C>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.3319-1674C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7309C>T
  hgvsp: ENSP00000359801.6:p.Arg2437Trp
  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.3319-1674C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg2437Trp
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

6-56480971-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480971
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480971
    reference: chr 6
allele count: 3
allele frequency: 2.471943441934048e-5
allele num: 121362
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.4297-1689G>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.4831-1689G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1689G>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.4297-1689G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7294G>C
  hgvsp: ENSP00000359801.6:p.Asp2432His
  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.4297-1689G>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.3319-1689G>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.4297-1689G>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.4297-1689G>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.3319-1689G>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1689G>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3982
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp2432His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ

6-56480972-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480972
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480972
    reference: chr 6
allele count: 4
allele frequency: 3.295978905735003e-5
allele num: 121360
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.3319-1690T>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.4297-1690T>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.4297-1690T>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.3319-1690T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7293T>C
  hgvsp: ENST00000370765.6:c.7293T>C(p.%3D)
  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.4297-1690T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1690T>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.4297-1690T>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.4831-1690T>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.4297-1690T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1690T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala2431Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/6-56480975-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480975
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480975
    reference: chr 6
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
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.4831-1693T>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.4297-1693T>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.3319-1693T>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.4297-1693T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1693T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7290T>G
  hgvsp: ENST00000370765.6:c.7290T>G(p.%3D)
  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.3319-1693T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1693T>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.4297-1693T>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.4297-1693T>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.4297-1693T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu2430Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

6-56480981-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480981
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480981
    reference: chr 6
allele count: 41
allele frequency: 3.37843405461527e-4
allele num: 121358
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.4831-1699A>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.3319-1699A>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.4297-1699A>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.4297-1699A>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.3319-1699A>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.4297-1699A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1699A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7284A>G
  hgvsp: ENST00000370765.6:c.7284A>G(p.%3D)
  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.4297-1699A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1699A>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.4297-1699A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr2428Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-56480981-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480981
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480981
    reference: chr 6
allele count: 8
allele frequency: 6.592066448029797e-5
allele num: 121358
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.3319-1699A>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.4297-1699A>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.4297-1699A>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.4831-1699A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1699A>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.4297-1699A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7284A>C
  hgvsp: ENST00000370765.6:c.7284A>C(p.%3D)
  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.4297-1699A>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.4297-1699A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1699A>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.3319-1699A>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr2428Thr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

6-56480984-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56480984
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56480984
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.3319-1702T>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.3319-1702T>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.4297-1702T>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.4297-1702T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.3319-1702T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.4417-1702T>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.4297-1702T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.7281T>C
  hgvsp: ENST00000370765.6:c.7281T>C(p.%3D)
  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.4297-1702T>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.4831-1702T>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.4297-1702T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu2427Leu
num of homozygotes: 0
reference allele: A

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

GenotypeQuality
all individuals: 8259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10407
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24752
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4006
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5068
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 7.677e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 1.884292e6

VQSLOD
type: SiteQuality
SIO_000300: -5.769e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.78e-1

QD
type: SiteQuality
SIO_000300: 8.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5064
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10409
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8262
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4005
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24748
bin: 6.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.683e0

DP
type: SiteQuality
SIO_000300: 1.884402e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.73e0

VQSLOD
type: SiteQuality
SIO_000300: -1.209e0

MQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

QD
type: SiteQuality
SIO_000300: 2.082e1

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

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

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

GenotypeQuality
all individuals: 1856
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8260
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variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5061
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2330
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4005
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.991458114790949e-5
allele num: 66730
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.29e-1

QD
type: SiteQuality
SIO_000300: 1.492e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.32e-1

DP
type: SiteQuality
SIO_000300: 1.884872e6

MQ
type: SiteQuality
SIO_000300: 5.984e1

FS
type: SiteQuality
SIO_000300: 5.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 24752
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10419
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4005
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8258
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3905
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5062
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.249279261964251e-3
allele num: 10406
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 1.535e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.838e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.86e-2

DP
type: SiteQuality
SIO_000300: 1.885773e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4006
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8265
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10412
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3898
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5065
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.765e0

MQRankSum
type: SiteQuality
SIO_000300: -1.846e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.127e0

QD
type: SiteQuality
SIO_000300: 1.386e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 8.106999999999999e0

DP
type: SiteQuality
SIO_000300: 1.885071e6

GenotypeQuality
all individuals: 3896
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

GenotypeQuality
all individuals: 8262
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10412
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

FS
type: SiteQuality
SIO_000300: 4.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

VQSLOD
type: SiteQuality
SIO_000300: 8.32e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 6.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.884981e6

MQRankSum
type: SiteQuality
SIO_000300: -3.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 24741
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10413
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variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3897
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1857
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 8262
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.265e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.648e1

DP
type: SiteQuality
SIO_000300: 1.88494e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.36e0

VQSLOD
type: SiteQuality
SIO_000300: -7.927e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

GenotypeQuality
all individuals: 24714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 4007
bin: 8.25e1
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 10
allele frequency: 1.498531439189594e-4
allele num: 66732
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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FS
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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SIO_000300: -4.481e0

ReadPosRankSum
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SIO_000300: 3.24e-1

DP
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MQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10400
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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Other
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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DP
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SIO_000300: 1.885032e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 5.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

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

Latino
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allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
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East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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allele num: 16510
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MQRankSum
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DP
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ClippingRankSum
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MQ
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FS
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VQSLOD
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QD
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10400
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
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Other
type: Population
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allele frequency: 0.0e0
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Latino
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

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

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

Other
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num of homozygotes: 0

South Asian
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FS
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MQ
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

East Asian
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African
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allele frequency: 0.0e0
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Other
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Latino
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allele frequency: 0.0e0
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South Asian
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VQSLOD
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

East Asian
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Latino
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African
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Other
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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East Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498531439189594e-5
allele num: 66732
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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MQ
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ClippingRankSum
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SIO_000300: 2.38e-1

MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.0e-4

FS
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SIO_000300: 3.64e0

VQSLOD
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SIO_000300: 7.77e-1

QD
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SIO_000300: 1.103e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.6e-1

DP
type: SiteQuality
SIO_000300: 1.884895e6

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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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

Other
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BaseQRankSum
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QD
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MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
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ClippingRankSum
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SIO_000300: 5.0e-3

ReadPosRankSum
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DP
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

QD
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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SIO_000300: 2.0e-4

MQ
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SIO_000300: 6.0e1

MQRankSum
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DP
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SIO_000300: 1.88479e6

ReadPosRankSum
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SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.33e0

ReadPosRankSum
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SIO_000300: 1.62e0

BaseQRankSum
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MQRankSum
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SIO_000300: 5.74e-1

InbreedingCoeff
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QD
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DP
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ClippingRankSum
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SIO_000300: -1.0e-1

VQSLOD
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SIO_000300: 2.41e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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ClippingRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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num of homozygotes: 0

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

Latino
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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: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

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

African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66722
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Latino
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South Asian
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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DP
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 2.997422216893472e-5
allele num: 66724
num of homozygotes: 0

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

East Asian
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Latino
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num of homozygotes: 0

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

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

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 frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

South Asian
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FS
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BaseQRankSum
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MQRankSum
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MQ
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DP
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ClippingRankSum
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.4e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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Latino
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allele frequency: 8.661008141347653e-5
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European (Finnish)
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African
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10366
num of homozygotes: 0

European (Finnish)
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East Asian
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Other
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Latino
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allele num: 11550
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South Asian
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European (Non-Finnish)
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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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 frequency: 5.994844433786943e-5
allele num: 66724
num of homozygotes: 0

Latino
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allele num: 11546
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African
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allele frequency: 1.697203471552556e-2
allele num: 10370
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South Asian
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Other
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East Asian
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QD
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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FS
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SIO_000300: 5.19e-1

BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.04e-1

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

African
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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Other
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Latino
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

Latino
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African
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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FS
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MQ
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QD
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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Other
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Latino
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African
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European (Finnish)
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FS
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DP
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BaseQRankSum
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MQRankSum
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QD
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SIO_000300: 1.06e1

ReadPosRankSum
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SIO_000300: 2.29e0

VQSLOD
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SIO_000300: 1.01e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.301e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66724
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 3.29e0

VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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DP
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MQ
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -1.615e0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66722
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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DP
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SIO_000300: 1.884037e6

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

VQSLOD
type: SiteQuality
SIO_000300: 3.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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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: 66718
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: -3.62e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

BaseQRankSum
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SIO_000300: -6.101e0

FS
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SIO_000300: 3.266e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.17e-1

DP
type: SiteQuality
SIO_000300: 1.883395e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.82e-1

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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QD
type: SiteQuality
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VQSLOD
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FS
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -4.034e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66722
num of homozygotes: 0

East Asian
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South Asian
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Latino
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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MQRankSum
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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DP
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MQ
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Latino
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African
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South Asian
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East Asian
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Other
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European (Non-Finnish)
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allele frequency: 1.498756032493031e-5
allele num: 66722
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InbreedingCoeff
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MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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African
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East Asian
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Latino
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European (Non-Finnish)
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allele num: 66722
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South Asian
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10352
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European (Non-Finnish)
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allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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SIO_000300: -2.05e-1

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

East Asian
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Latino
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allele frequency: 8.656509695290859e-5
allele num: 11552
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African
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allele num: 10348
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

European (Finnish)
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QD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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SIO_000300: -8.852e-1

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

South Asian
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allele num: 16510
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Other
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.655011251514626e-5
allele num: 11554
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East Asian
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European (Non-Finnish)
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allele num: 66722
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MQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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DP
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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East Asian
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African
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Other
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European (Non-Finnish)
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allele num: 66720
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South Asian
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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QD
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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East Asian
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European (Non-Finnish)
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allele num: 66710
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Latino
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African
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Other
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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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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Other
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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MQRankSum
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FS
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.97e1

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

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8174
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

FS
type: SiteQuality
SIO_000300: 2.328e0

VQSLOD
type: SiteQuality
SIO_000300: 6.919999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.446e0

DP
type: SiteQuality
SIO_000300: 1.882836e6

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeQuality
all individuals: 117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.883033e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 3.598e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.376e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

MQRankSum
type: SiteQuality
SIO_000300: -4.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e-1

QD
type: SiteQuality
SIO_000300: 1.58e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10493
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1859
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.883307e6

FS
type: SiteQuality
SIO_000300: 4.572e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.997e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.894e0

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

QD
type: SiteQuality
SIO_000300: 1.675e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.01e0

GenotypeQuality
all individuals: 3872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8183
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.412e0

MQRankSum
type: SiteQuality
SIO_000300: -1.941e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.504e1

FS
type: SiteQuality
SIO_000300: 8.99e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

DP
type: SiteQuality
SIO_000300: 1.883647e6

VQSLOD
type: SiteQuality
SIO_000300: -1.759e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2328
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5040
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.342e0

FS
type: SiteQuality
SIO_000300: 2.296e0

VQSLOD
type: SiteQuality
SIO_000300: -2.314e-1

DP
type: SiteQuality
SIO_000300: 1.884359e6

QD
type: SiteQuality
SIO_000300: 1.565e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

GenotypeQuality
all individuals: 24712
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0144e1

QD
type: SiteQuality
SIO_000300: 1.485e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.756e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

DP
type: SiteQuality
SIO_000300: 1.885714e6

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.275e0

VQSLOD
type: SiteQuality
SIO_000300: -2.404e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24750
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.758e0

QD
type: SiteQuality
SIO_000300: 1.376e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 1.2858e1

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.886178e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.711e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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Other
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African
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East Asian
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European (Finnish)
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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Latino
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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Latino
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South Asian
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ClippingRankSum
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VQSLOD
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QD
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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Latino
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African
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South Asian
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DP
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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Latino
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European (Non-Finnish)
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South Asian
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DP
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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African
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South Asian
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Latino
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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South Asian
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QD
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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VQSLOD
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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BaseQRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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East Asian
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Latino
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allele num: 11548
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Other
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European (Non-Finnish)
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: 1.51e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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VQSLOD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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QD
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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Other
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African
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Latino
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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Other
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South Asian
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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African
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VQSLOD
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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QD
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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BaseQRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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QD
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FS
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DP
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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Latino
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European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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DP
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BaseQRankSum
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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