http://identifiers.org/exac.variant/6-56492939-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492939
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492939
    reference: chr 6
allele count: 3
allele frequency: 2.473084595980413e-5
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2885T>G
  hgvsp: ENSP00000404924.1:p.Ile962Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3863T>G
  hgvsp: ENSP00000354508.3:p.Ile1288Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2885T>G
  hgvsp: ENSP00000244364.6:p.Ile962Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2885T>G
  hgvsp: ENSP00000393645.2:p.Ile962Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3863T>G
  hgvsp: ENSP00000400883.2:p.Ile1288Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3983T>G
  hgvsp: ENSP00000431030.1:p.Ile1328Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2885T>G
  hgvsp: ENSP00000431003.1:p.Ile962Ser
  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.2885T>G
  hgvsp: ENSP00000359801.6:p.Ile962Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4397T>G
  hgvsp: ENSP00000359790.5:p.Ile1466Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3863T>G
  hgvsp: ENSP00000359824.2:p.Ile1288Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3863T>G
  hgvsp: ENSP00000307959.6:p.Ile1288Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3863T>G
  hgvsp: ENSP00000359805.4:p.Ile1288Ser
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile962Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/6-56492942-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492942
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492942
    reference: chr 6
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3860G>T
  hgvsp: ENSP00000307959.6:p.Gly1287Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2882G>T
  hgvsp: ENSP00000244364.6:p.Gly961Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3860G>T
  hgvsp: ENSP00000354508.3:p.Gly1287Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2882G>T
  hgvsp: ENSP00000431003.1:p.Gly961Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3980G>T
  hgvsp: ENSP00000431030.1:p.Gly1327Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3860G>T
  hgvsp: ENSP00000400883.2:p.Gly1287Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4394G>T
  hgvsp: ENSP00000359790.5:p.Gly1465Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3860G>T
  hgvsp: ENSP00000359824.2:p.Gly1287Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2882G>T
  hgvsp: ENSP00000393645.2:p.Gly961Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3860G>T
  hgvsp: ENSP00000359805.4:p.Gly1287Val
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2882G>T
  hgvsp: ENSP00000404924.1:p.Gly961Val
  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.2882G>T
  hgvsp: ENSP00000359801.6:p.Gly961Val
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14451
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly961Val
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

6-56492955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492955
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492955
    reference: chr 6
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
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.2869C>T
  hgvsp: ENSP00000359801.6:p.Arg957Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3847C>T
  hgvsp: ENSP00000400883.2:p.Arg1283Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2869C>T
  hgvsp: ENSP00000404924.1:p.Arg957Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3847C>T
  hgvsp: ENSP00000359805.4:p.Arg1283Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2869C>T
  hgvsp: ENSP00000393645.2:p.Arg957Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3847C>T
  hgvsp: ENSP00000359824.2:p.Arg1283Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2869C>T
  hgvsp: ENSP00000244364.6:p.Arg957Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4381C>T
  hgvsp: ENSP00000359790.5:p.Arg1461Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3847C>T
  hgvsp: ENSP00000354508.3:p.Arg1283Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3967C>T
  hgvsp: ENSP00000431030.1:p.Arg1323Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2869C>T
  hgvsp: ENSP00000431003.1:p.Arg957Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3847C>T
  hgvsp: ENSP00000307959.6:p.Arg1283Trp
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5967
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg957Trp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

6-56492959-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492959
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492959
    reference: chr 6
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865G>C
  hgvsp: ENSP00000431003.1:p.Arg955Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2865G>C
  hgvsp: ENSP00000393645.2:p.Arg955Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3843G>C
  hgvsp: ENSP00000400883.2:p.Arg1281Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4377G>C
  hgvsp: ENSP00000359790.5:p.Arg1459Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3843G>C
  hgvsp: ENSP00000359805.4:p.Arg1281Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3963G>C
  hgvsp: ENSP00000431030.1:p.Arg1321Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2865G>C
  hgvsp: ENSP00000404924.1:p.Arg955Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2865G>C
  hgvsp: ENSP00000244364.6:p.Arg955Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3843G>C
  hgvsp: ENSP00000354508.3:p.Arg1281Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3843G>C
  hgvsp: ENSP00000307959.6:p.Arg1281Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865G>C
  hgvsp: ENSP00000359801.6:p.Arg955Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3843G>C
  hgvsp: ENSP00000359824.2:p.Arg1281Ser
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg955Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

6-56492964-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492964
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492964
    reference: chr 6
allele count: 2
allele frequency: 1.650873311982039e-5
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3843-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2865-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3843-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2865-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4377-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3843-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3843-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3963-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2865-5C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3843-5C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14353
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.2865-5C>T
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

6-56492964-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492964
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492964
    reference: chr 6
allele count: 2
allele frequency: 1.650873311982039e-5
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3963-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2865-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4377-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3843-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3843-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3843-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3843-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2865-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2865-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865-5C>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3843-5C>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5944
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2865-5C>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

6-56492976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492976
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492976
    reference: chr 6
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865-17G>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.3843-17G>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.3843-17G>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.3963-17G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865-17G>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.3843-17G>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.3843-17G>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.2865-17G>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.3843-17G>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.2865-17G>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.4377-17G>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.2865-17G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

6-56492977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492977
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492977
    reference: chr 6
allele count: 7
allele frequency: 5.789717461787865e-5
allele num: 120904
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.2865-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3843-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3843-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4377-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3843-18C>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.3843-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3843-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2865-18C>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.3963-18C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2865-18C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13959
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

6-56492987-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492987
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492987
    reference: chr 6
allele count: 3
allele frequency: 2.486531288852051e-5
allele num: 120650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3843-28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3843-28C>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.3963-28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865-28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2865-28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2865-28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3843-28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3843-28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865-28C>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.2865-28C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3843-28C>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.4377-28C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6271
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5733
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/6-56492993-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492993
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492993
    reference: chr 6
allele count: 2
allele frequency: 1.659227795384028e-5
allele num: 120538
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.3963-34G>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.2865-34G>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.2865-34G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865-34G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865-34G>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.3843-34G>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.3843-34G>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.2865-34G>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.4377-34G>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.3843-34G>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.3843-34G>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.3843-34G>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17919
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-56492996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492996
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492996
    reference: chr 6
allele count: 1
allele frequency: 8.306199747491528e-6
allele num: 120392
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.2865-37G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865-37G>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.3843-37G>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.3843-37G>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.2865-37G>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.3843-37G>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.2865-37G>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.3963-37G>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.3843-37G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865-37G>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.4377-37G>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.3843-37G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11040
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

6-56492997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56492997
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56492997
    reference: chr 6
allele count: 42
allele frequency: 3.487618952717851e-4
allele num: 120426
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.4377-38C>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.3843-38C>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.3963-38C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865-38C>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.3843-38C>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.3843-38C>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.2865-38C>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.3843-38C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865-38C>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.3843-38C>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.2865-38C>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.2865-38C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17097
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10876
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS

6-56493001-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56493001
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56493001
    reference: chr 6
allele count: 1
allele frequency: 8.306475728477921e-6
allele num: 120388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2865-42A>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.4377-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3843-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3843-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2865-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3843-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3843-42A>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.3963-42A>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.2865-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2865-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3843-42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2865-42A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15483
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP

6-56493997-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56493997
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56493997
    reference: chr 6
allele count: 261
allele frequency: 2.153465346534654e-3
allele num: 121200
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.2864+51G>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.3842+51G>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.3842+51G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+51G>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.3842+51G>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.2864+51G>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.3842+51G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+51G>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.4376+51G>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.3842+51G>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.3962+51G>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.2864+51G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8085
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 13008
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27207
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 9.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
num of homozygotes: 2
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

6-56493997-CATAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56493997
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56493993
    reference: chr 6
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
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.3842+47_3842+50delCTAT
  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.3962+47_3962+50delCTAT
  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.2864+47_2864+50delCTAT
  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.3842+47_3842+50delCTAT
  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.4376+47_4376+50delCTAT
  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.3842+47_3842+50delCTAT
  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.2864+47_2864+50delCTAT
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+47_2864+50delCTAT
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+47_2864+50delCTAT
  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.2864+47_2864+50delCTAT
  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.3842+47_3842+50delCTAT
  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.3842+47_3842+50delCTAT
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: CATAG
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

6-56494003-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494003
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494003
    reference: chr 6
allele count: 12
allele frequency: 9.897233723174372e-5
allele num: 121246
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.3842+45A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+45A>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.3842+45A>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.3842+45A>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.4376+45A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+45A>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.2864+45A>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.3842+45A>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.3842+45A>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.3962+45A>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.2864+45A>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.2864+45A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27278
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

6-56494005-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494005
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494005
    reference: chr 6
allele count: 3
allele frequency: 2.474063566939913e-5
allele num: 121258
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.3962+43C>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.4376+43C>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.2864+43C>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.2864+43C>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.3842+43C>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.3842+43C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+43C>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.2864+43C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+43C>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.3842+43C>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.3842+43C>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.3842+43C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

6-56494009-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494009
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494009
    reference: chr 6
allele count: 3
allele frequency: 2.473818751546137e-5
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+39A>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.2864+39A>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.3962+39A>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.3842+39A>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.4376+39A>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.3842+39A>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.3842+39A>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.3842+39A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+39A>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.2864+39A>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.2864+39A>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.3842+39A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27339
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

6-56494010-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494010
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494010
    reference: chr 6
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3842+38A>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.3842+38A>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.2864+38A>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.3842+38A>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.2864+38A>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.3842+38A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+38A>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.3842+38A>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.4376+38A>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.3962+38A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+38A>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.2864+38A>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/6-56494012-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494012
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494012
    reference: chr 6
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3842+36T>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.3842+36T>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.3962+36T>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.2864+36T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+36T>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+36T>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.2864+36T>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.3842+36T>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.4376+36T>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.3842+36T>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.2864+36T>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.3842+36T>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13019
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

6-56494018-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494018
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494018
    reference: chr 6
allele count: 3
allele frequency: 2.473125370968806e-5
allele num: 121304
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.2864+30A>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.3842+30A>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.3842+30A>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.3842+30A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+30A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+30A>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.2864+30A>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.4376+30A>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.2864+30A>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.3962+30A>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.3842+30A>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.3842+30A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-56494027-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494027
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494027
    reference: chr 6
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3842+21A>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.2864+21A>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.2864+21A>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.3842+21A>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.2864+21A>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.3842+21A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+21A>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+21A>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.3842+21A>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.4376+21A>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.3962+21A>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.3842+21A>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/6-56494031-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494031
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494032
    reference: chr 6
allele count: 8
allele frequency: 6.592175088170342e-5
allele num: 121356
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4376+16dupT
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+16dupT
  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.2864+16dupT
  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.3842+16dupT
  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.3842+16dupT
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+16dupT
  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.2864+16dupT
  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.2864+16dupT
  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.3842+16dupT
  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.3842+16dupT
  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.3842+16dupT
  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.3962+16dupT
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

6-56494033-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494033
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494033
    reference: chr 6
allele count: 261
allele frequency: 2.150697122515574e-3
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4376+15T>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.2864+15T>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.3842+15T>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.2864+15T>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.3962+15T>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2864+15T>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.3842+15T>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.3842+15T>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.2864+15T>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.3842+15T>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2864+15T>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.3842+15T>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 27426
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 8471
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 2
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

6-56494049-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494049
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494049
    reference: chr 6
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2863A>G
  hgvsp: ENSP00000431003.1:p.Arg955Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4375A>G
  hgvsp: ENSP00000359790.5:p.Arg1459Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3961A>G
  hgvsp: ENSP00000431030.1:p.Arg1321Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2863A>G
  hgvsp: ENSP00000359801.6:p.Arg955Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3841A>G
  hgvsp: ENSP00000359824.2:p.Arg1281Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2863A>G
  hgvsp: ENSP00000244364.6:p.Arg955Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3841A>G
  hgvsp: ENSP00000307959.6:p.Arg1281Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2863A>G
  hgvsp: ENSP00000393645.2:p.Arg955Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3841A>G
  hgvsp: ENSP00000359805.4:p.Arg1281Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3841A>G
  hgvsp: ENSP00000354508.3:p.Arg1281Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3841A>G
  hgvsp: ENSP00000400883.2:p.Arg1281Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2863A>G
  hgvsp: ENSP00000404924.1:p.Arg955Gly
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg955Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

6-56494050-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494050
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494050
    reference: chr 6
allele count: 10
allele frequency: 8.2387253044209e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2862C>T
  hgvsp: ENST00000244364.6:c.2862C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2862C>T
  hgvsp: ENST00000370765.6:c.2862C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3840C>T
  hgvsp: ENST00000312431.6:c.3840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2862C>T
  hgvsp: ENST00000518935.1:c.2862C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2862C>T
  hgvsp: ENST00000439203.1:c.2862C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3840C>T
  hgvsp: ENST00000370788.2:c.3840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3840C>T
  hgvsp: ENST00000370769.4:c.3840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2862C>T
  hgvsp: ENST00000446842.2:c.2862C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3960C>T
  hgvsp: ENST00000520645.1:c.3960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4374C>T
  hgvsp: ENST00000370754.5:c.4374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3840C>T
  hgvsp: ENST00000421834.2:c.3840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3840C>T
  hgvsp: ENST00000361203.3:c.3840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2862C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-56494055-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494055
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494055
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3835G>C
  hgvsp: ENSP00000400883.2:p.Asp1279His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3835G>C
  hgvsp: ENSP00000354508.3:p.Asp1279His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2857G>C
  hgvsp: ENSP00000431003.1:p.Asp953His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3835G>C
  hgvsp: ENSP00000307959.6:p.Asp1279His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4369G>C
  hgvsp: ENSP00000359790.5:p.Asp1457His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3835G>C
  hgvsp: ENSP00000359824.2:p.Asp1279His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2857G>C
  hgvsp: ENSP00000393645.2:p.Asp953His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3835G>C
  hgvsp: ENSP00000359805.4:p.Asp1279His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2857G>C
  hgvsp: ENSP00000404924.1:p.Asp953His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3955G>C
  hgvsp: ENSP00000431030.1:p.Asp1319His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2857G>C
  hgvsp: ENSP00000244364.6:p.Asp953His
  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.2857G>C
  hgvsp: ENSP00000359801.6:p.Asp953His
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp953His
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/6-56494059-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494059
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494059
    reference: chr 6
allele count: 8
allele frequency: 6.590871642774756e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2853G>T
  hgvsp: ENSP00000244364.6:p.Gln951His
  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.2853G>T
  hgvsp: ENSP00000359801.6:p.Gln951His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2853G>T
  hgvsp: ENSP00000393645.2:p.Gln951His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3831G>T
  hgvsp: ENSP00000307959.6:p.Gln1277His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2853G>T
  hgvsp: ENSP00000431003.1:p.Gln951His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3831G>T
  hgvsp: ENSP00000354508.3:p.Gln1277His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3831G>T
  hgvsp: ENSP00000359824.2:p.Gln1277His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4365G>T
  hgvsp: ENSP00000359790.5:p.Gln1455His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3831G>T
  hgvsp: ENSP00000359805.4:p.Gln1277His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2853G>T
  hgvsp: ENSP00000404924.1:p.Gln951His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3951G>T
  hgvsp: ENSP00000431030.1:p.Gln1317His
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3831G>T
  hgvsp: ENSP00000400883.2:p.Gln1277His
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln951His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

6-56494065-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494065
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494065
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3825T>C
  hgvsp: ENST00000312431.6:c.3825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3825T>C
  hgvsp: ENST00000361203.3:c.3825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3825T>C
  hgvsp: ENST00000370769.4:c.3825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2847T>C
  hgvsp: ENST00000518935.1:c.2847T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3825T>C
  hgvsp: ENST00000370788.2:c.3825T>C(p.%3D)
  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.2847T>C
  hgvsp: ENST00000370765.6:c.2847T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4359T>C
  hgvsp: ENST00000370754.5:c.4359T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2847T>C
  hgvsp: ENST00000439203.1:c.2847T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3825T>C
  hgvsp: ENST00000421834.2:c.3825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3945T>C
  hgvsp: ENST00000520645.1:c.3945T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2847T>C
  hgvsp: ENST00000244364.6:c.2847T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2847T>C
  hgvsp: ENST00000446842.2:c.2847T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His949His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

6-56494066-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494066
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494066
    reference: chr 6
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2846A>G
  hgvsp: ENSP00000404924.1:p.His949Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3824A>G
  hgvsp: ENSP00000354508.3:p.His1275Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2846A>G
  hgvsp: ENSP00000244364.6:p.His949Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2846A>G
  hgvsp: ENSP00000393645.2:p.His949Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3824A>G
  hgvsp: ENSP00000359824.2:p.His1275Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3944A>G
  hgvsp: ENSP00000431030.1:p.His1315Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4358A>G
  hgvsp: ENSP00000359790.5:p.His1453Arg
  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.2846A>G
  hgvsp: ENSP00000359801.6:p.His949Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3824A>G
  hgvsp: ENSP00000359805.4:p.His1275Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3824A>G
  hgvsp: ENSP00000307959.6:p.His1275Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2846A>G
  hgvsp: ENSP00000431003.1:p.His949Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3824A>G
  hgvsp: ENSP00000400883.2:p.His1275Arg
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His949Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

6-56494067-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494067
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494067
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2845C>A
  hgvsp: ENSP00000393645.2:p.His949Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3823C>A
  hgvsp: ENSP00000354508.3:p.His1275Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3823C>A
  hgvsp: ENSP00000307959.6:p.His1275Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2845C>A
  hgvsp: ENSP00000404924.1:p.His949Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3823C>A
  hgvsp: ENSP00000400883.2:p.His1275Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2845C>A
  hgvsp: ENSP00000431003.1:p.His949Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3943C>A
  hgvsp: ENSP00000431030.1:p.His1315Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2845C>A
  hgvsp: ENSP00000244364.6:p.His949Asn
  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.2845C>A
  hgvsp: ENSP00000359801.6:p.His949Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3823C>A
  hgvsp: ENSP00000359824.2:p.His1275Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4357C>A
  hgvsp: ENSP00000359790.5:p.His1453Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3823C>A
  hgvsp: ENSP00000359805.4:p.His1275Asn
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His949Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

6-56494071-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494071
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494071
    reference: chr 6
allele count: 2871
allele frequency: 2.365026278069756e-2
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2841T>C
  hgvsp: ENST00000370765.6:c.2841T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2841T>C
  hgvsp: ENST00000518935.1:c.2841T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2841T>C
  hgvsp: ENST00000244364.6:c.2841T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3819T>C
  hgvsp: ENST00000312431.6:c.3819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3819T>C
  hgvsp: ENST00000361203.3:c.3819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2841T>C
  hgvsp: ENST00000446842.2:c.2841T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3819T>C
  hgvsp: ENST00000370769.4:c.3819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3819T>C
  hgvsp: ENST00000421834.2:c.3819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2841T>C
  hgvsp: ENST00000439203.1:c.2841T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3819T>C
  hgvsp: ENST00000370788.2:c.3819T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4353T>C
  hgvsp: ENST00000370754.5:c.4353T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3939T>C
  hgvsp: ENST00000520645.1:c.3939T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12804
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 9.75e1
  variant carriers: 2251
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
hgvs: p.Asn947Asn
num of homozygotes: 44
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-56494072-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494072
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494072
    reference: chr 6
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
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.2840A>G
  hgvsp: ENSP00000359801.6:p.Asn947Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2840A>G
  hgvsp: ENSP00000431003.1:p.Asn947Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3818A>G
  hgvsp: ENSP00000359824.2:p.Asn1273Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2840A>G
  hgvsp: ENSP00000393645.2:p.Asn947Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3818A>G
  hgvsp: ENSP00000400883.2:p.Asn1273Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3818A>G
  hgvsp: ENSP00000307959.6:p.Asn1273Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2840A>G
  hgvsp: ENSP00000244364.6:p.Asn947Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3818A>G
  hgvsp: ENSP00000359805.4:p.Asn1273Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3938A>G
  hgvsp: ENSP00000431030.1:p.Asn1313Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4352A>G
  hgvsp: ENSP00000359790.5:p.Asn1451Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2840A>G
  hgvsp: ENSP00000404924.1:p.Asn947Ser
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3818A>G
  hgvsp: ENSP00000354508.3:p.Asn1273Ser
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn947Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

6-56494092-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494092
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494092
    reference: chr 6
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2820A>G
  hgvsp: ENST00000439203.1:c.2820A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3798A>G
  hgvsp: ENST00000370788.2:c.3798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3798A>G
  hgvsp: ENST00000361203.3:c.3798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3798A>G
  hgvsp: ENST00000421834.2:c.3798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3798A>G
  hgvsp: ENST00000370769.4:c.3798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2820A>G
  hgvsp: ENST00000244364.6:c.2820A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3798A>G
  hgvsp: ENST00000312431.6:c.3798A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4332A>G
  hgvsp: ENST00000370754.5:c.4332A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2820A>G
  hgvsp: ENST00000446842.2:c.2820A>G(p.%3D)
  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.2820A>G
  hgvsp: ENST00000370765.6:c.2820A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2820A>G
  hgvsp: ENST00000518935.1:c.2820A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3918A>G
  hgvsp: ENST00000520645.1:c.3918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln940Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

6-56494130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494130
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494130
    reference: chr 6
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2782G>A
  hgvsp: ENSP00000431003.1:p.Asp928Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3760G>A
  hgvsp: ENSP00000400883.2:p.Asp1254Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4294G>A
  hgvsp: ENSP00000359790.5:p.Asp1432Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2782G>A
  hgvsp: ENSP00000393645.2:p.Asp928Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3760G>A
  hgvsp: ENSP00000359805.4:p.Asp1254Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3760G>A
  hgvsp: ENSP00000359824.2:p.Asp1254Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3760G>A
  hgvsp: ENSP00000354508.3:p.Asp1254Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3760G>A
  hgvsp: ENSP00000307959.6:p.Asp1254Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2782G>A
  hgvsp: ENSP00000404924.1:p.Asp928Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3880G>A
  hgvsp: ENSP00000431030.1:p.Asp1294Asn
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2782G>A
  hgvsp: ENSP00000244364.6:p.Asp928Asn
  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.2782G>A
  hgvsp: ENSP00000359801.6:p.Asp928Asn
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp928Asn
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

6-56494132-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494132
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494132
    reference: chr 6
allele count: 2
allele frequency: 1.647555028337947e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3758G>A
  hgvsp: ENSP00000359824.2:p.Arg1253Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3878G>A
  hgvsp: ENSP00000431030.1:p.Arg1293Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3758G>A
  hgvsp: ENSP00000359805.4:p.Arg1253Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2780G>A
  hgvsp: ENSP00000244364.6:p.Arg927Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2780G>A
  hgvsp: ENSP00000431003.1:p.Arg927Gln
  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.2780G>A
  hgvsp: ENSP00000359801.6:p.Arg927Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3758G>A
  hgvsp: ENSP00000307959.6:p.Arg1253Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4292G>A
  hgvsp: ENSP00000359790.5:p.Arg1431Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2780G>A
  hgvsp: ENSP00000393645.2:p.Arg927Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3758G>A
  hgvsp: ENSP00000354508.3:p.Arg1253Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2780G>A
  hgvsp: ENSP00000404924.1:p.Arg927Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3758G>A
  hgvsp: ENSP00000400883.2:p.Arg1253Gln
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg927Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

6-56494133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494133
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494133
    reference: chr 6
allele count: 4
allele frequency: 3.295218637756615e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4291C>T
  hgvsp: ENSP00000359790.5:p.Arg1431Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2779C>T
  hgvsp: ENSP00000431003.1:p.Arg927Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2779C>T
  hgvsp: ENSP00000393645.2:p.Arg927Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2779C>T
  hgvsp: ENSP00000404924.1:p.Arg927Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2779C>T
  hgvsp: ENSP00000244364.6:p.Arg927Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3757C>T
  hgvsp: ENSP00000354508.3:p.Arg1253Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3757C>T
  hgvsp: ENSP00000359824.2:p.Arg1253Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3757C>T
  hgvsp: ENSP00000307959.6:p.Arg1253Trp
  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.2779C>T
  hgvsp: ENSP00000359801.6:p.Arg927Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3757C>T
  hgvsp: ENSP00000359805.4:p.Arg1253Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3877C>T
  hgvsp: ENSP00000431030.1:p.Arg1293Trp
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3757C>T
  hgvsp: ENSP00000400883.2:p.Arg1253Trp
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg927Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

6-56494141-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494141
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494141
    reference: chr 6
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3749A>G
  hgvsp: ENSP00000400883.2:p.Tyr1250Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2771A>G
  hgvsp: ENSP00000431003.1:p.Tyr924Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2771A>G
  hgvsp: ENSP00000404924.1:p.Tyr924Cys
  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.2771A>G
  hgvsp: ENSP00000359801.6:p.Tyr924Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3749A>G
  hgvsp: ENSP00000359805.4:p.Tyr1250Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3749A>G
  hgvsp: ENSP00000359824.2:p.Tyr1250Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3869A>G
  hgvsp: ENSP00000431030.1:p.Tyr1290Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2771A>G
  hgvsp: ENSP00000393645.2:p.Tyr924Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4283A>G
  hgvsp: ENSP00000359790.5:p.Tyr1428Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2771A>G
  hgvsp: ENSP00000244364.6:p.Tyr924Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3749A>G
  hgvsp: ENSP00000307959.6:p.Tyr1250Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3749A>G
  hgvsp: ENSP00000354508.3:p.Tyr1250Cys
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13421
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr924Cys
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: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

6-56494143-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494143
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494143
    reference: chr 6
allele count: 3
allele frequency: 2.471699045924168e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3747G>A
  hgvsp: ENST00000421834.2:c.3747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3867G>A
  hgvsp: ENST00000520645.1:c.3867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3747G>A
  hgvsp: ENST00000361203.3:c.3747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2769G>A
  hgvsp: ENST00000518935.1:c.2769G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3747G>A
  hgvsp: ENST00000370769.4:c.3747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2769G>A
  hgvsp: ENST00000439203.1:c.2769G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2769G>A
  hgvsp: ENST00000244364.6:c.2769G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2769G>A
  hgvsp: ENST00000446842.2:c.2769G>A(p.%3D)
  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.2769G>A
  hgvsp: ENST00000370765.6:c.2769G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4281G>A
  hgvsp: ENST00000370754.5:c.4281G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3747G>A
  hgvsp: ENST00000370788.2:c.3747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3747G>A
  hgvsp: ENST00000312431.6:c.3747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28648
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr923Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

6-56494154-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494154
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494154
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2758A>C
  hgvsp: ENSP00000431003.1:p.Met920Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3856A>C
  hgvsp: ENSP00000431030.1:p.Met1286Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3736A>C
  hgvsp: ENSP00000359824.2:p.Met1246Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2758A>C
  hgvsp: ENSP00000244364.6:p.Met920Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3736A>C
  hgvsp: ENSP00000307959.6:p.Met1246Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2758A>C
  hgvsp: ENSP00000393645.2:p.Met920Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4270A>C
  hgvsp: ENSP00000359790.5:p.Met1424Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2758A>C
  hgvsp: ENSP00000404924.1:p.Met920Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3736A>C
  hgvsp: ENSP00000400883.2:p.Met1246Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3736A>C
  hgvsp: ENSP00000359805.4:p.Met1246Leu
  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.2758A>C
  hgvsp: ENSP00000359801.6:p.Met920Leu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3736A>C
  hgvsp: ENSP00000354508.3:p.Met1246Leu
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met920Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

6-56494158-ATCAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494158
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494154
    reference: chr 6
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3848_3851delGTGA
  hgvsp: ENSP00000431030.1:p.Ser1283MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3728_3731delGTGA
  hgvsp: ENSP00000400883.2:p.Ser1243MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2750_2753delGTGA
  hgvsp: ENSP00000404924.1:p.Ser917MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3728_3731delGTGA
  hgvsp: ENSP00000307959.6:p.Ser1243MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2750_2753delGTGA
  hgvsp: ENSP00000431003.1:p.Ser917MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4262_4265delGTGA
  hgvsp: ENSP00000359790.5:p.Ser1421MetfsTer24
  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.2750_2753delGTGA
  hgvsp: ENSP00000359801.6:p.Ser917MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3728_3731delGTGA
  hgvsp: ENSP00000359824.2:p.Ser1243MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3728_3731delGTGA
  hgvsp: ENSP00000359805.4:p.Ser1243MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2750_2753delGTGA
  hgvsp: ENSP00000393645.2:p.Ser917MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2750_2753delGTGA
  hgvsp: ENSP00000244364.6:p.Ser917MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3728_3731delGTGA
  hgvsp: ENSP00000354508.3:p.Ser1243MetfsTer24
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser917MetfsTer24
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: ATCAC
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

6-56494178-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494178
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494178
    reference: chr 6
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4246A>C
  hgvsp: ENSP00000359790.5:p.Lys1416Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2734A>C
  hgvsp: ENSP00000431003.1:p.Lys912Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3712A>C
  hgvsp: ENSP00000400883.2:p.Lys1238Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3832A>C
  hgvsp: ENSP00000431030.1:p.Lys1278Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2734A>C
  hgvsp: ENSP00000393645.2:p.Lys912Gln
  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.2734A>C
  hgvsp: ENSP00000359801.6:p.Lys912Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3712A>C
  hgvsp: ENSP00000359824.2:p.Lys1238Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2734A>C
  hgvsp: ENSP00000404924.1:p.Lys912Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2734A>C
  hgvsp: ENSP00000244364.6:p.Lys912Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3712A>C
  hgvsp: ENSP00000359805.4:p.Lys1238Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3712A>C
  hgvsp: ENSP00000307959.6:p.Lys1238Gln
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3712A>C
  hgvsp: ENSP00000354508.3:p.Lys1238Gln
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys912Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

6-56494184-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494184
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494184
    reference: chr 6
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3706T>C
  hgvsp: ENST00000370788.2:c.3706T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3706T>C
  hgvsp: ENST00000361203.3:c.3706T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3706T>C
  hgvsp: ENST00000421834.2:c.3706T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4240T>C
  hgvsp: ENST00000370754.5:c.4240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3706T>C
  hgvsp: ENST00000370769.4:c.3706T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2728T>C
  hgvsp: ENST00000244364.6:c.2728T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2728T>C
  hgvsp: ENST00000439203.1:c.2728T>C(p.%3D)
  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.2728T>C
  hgvsp: ENST00000370765.6:c.2728T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2728T>C
  hgvsp: ENST00000518935.1:c.2728T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3706T>C
  hgvsp: ENST00000312431.6:c.3706T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3826T>C
  hgvsp: ENST00000520645.1:c.3826T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2728T>C
  hgvsp: ENST00000446842.2:c.2728T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu910Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

6-56494186-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494186
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494186
    reference: chr 6
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2726A>G
  hgvsp: ENSP00000393645.2:p.Glu909Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2726A>G
  hgvsp: ENSP00000431003.1:p.Glu909Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2726A>G
  hgvsp: ENSP00000244364.6:p.Glu909Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4238A>G
  hgvsp: ENSP00000359790.5:p.Glu1413Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3704A>G
  hgvsp: ENSP00000359824.2:p.Glu1235Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3824A>G
  hgvsp: ENSP00000431030.1:p.Glu1275Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3704A>G
  hgvsp: ENSP00000307959.6:p.Glu1235Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3704A>G
  hgvsp: ENSP00000359805.4:p.Glu1235Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3704A>G
  hgvsp: ENSP00000354508.3:p.Glu1235Gly
  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.2726A>G
  hgvsp: ENSP00000359801.6:p.Glu909Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2726A>G
  hgvsp: ENSP00000404924.1:p.Glu909Gly
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3704A>G
  hgvsp: ENSP00000400883.2:p.Glu1235Gly
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu909Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum

6-56494191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494191
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494191
    reference: chr 6
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3699G>A
  hgvsp: ENST00000421834.2:c.3699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3699G>A
  hgvsp: ENST00000370788.2:c.3699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2721G>A
  hgvsp: ENST00000439203.1:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3819G>A
  hgvsp: ENST00000520645.1:c.3819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3699G>A
  hgvsp: ENST00000370769.4:c.3699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2721G>A
  hgvsp: ENST00000446842.2:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2721G>A
  hgvsp: ENST00000518935.1:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4233G>A
  hgvsp: ENST00000370754.5:c.4233G>A(p.%3D)
  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.2721G>A
  hgvsp: ENST00000370765.6:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3699G>A
  hgvsp: ENST00000312431.6:c.3699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2721G>A
  hgvsp: ENST00000244364.6:c.2721G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3699G>A
  hgvsp: ENST00000361203.3:c.3699G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu907Glu
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: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-56494193-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494193
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494193
    reference: chr 6
allele count: 63
allele frequency: 5.193563279034492e-4
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3817G>A
  hgvsp: ENSP00000431030.1:p.Glu1273Lys
  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.2719G>A
  hgvsp: ENSP00000359801.6:p.Glu907Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4231G>A
  hgvsp: ENSP00000359790.5:p.Glu1411Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2719G>A
  hgvsp: ENSP00000431003.1:p.Glu907Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3697G>A
  hgvsp: ENSP00000400883.2:p.Glu1233Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2719G>A
  hgvsp: ENSP00000404924.1:p.Glu907Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3697G>A
  hgvsp: ENSP00000359805.4:p.Glu1233Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2719G>A
  hgvsp: ENSP00000393645.2:p.Glu907Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3697G>A
  hgvsp: ENSP00000359824.2:p.Glu1233Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3697G>A
  hgvsp: ENSP00000354508.3:p.Glu1233Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2719G>A
  hgvsp: ENSP00000244364.6:p.Glu907Lys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3697G>A
  hgvsp: ENSP00000307959.6:p.Glu1233Lys
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 28656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Glu907Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

6-56494209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494209
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494209
    reference: chr 6
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
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.2703G>A
  hgvsp: ENST00000370765.6:c.2703G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3801G>A
  hgvsp: ENST00000520645.1:c.3801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2703G>A
  hgvsp: ENST00000446842.2:c.2703G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2703G>A
  hgvsp: ENST00000244364.6:c.2703G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3681G>A
  hgvsp: ENST00000421834.2:c.3681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4215G>A
  hgvsp: ENST00000370754.5:c.4215G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3681G>A
  hgvsp: ENST00000361203.3:c.3681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2703G>A
  hgvsp: ENST00000518935.1:c.2703G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3681G>A
  hgvsp: ENST00000312431.6:c.3681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3681G>A
  hgvsp: ENST00000370788.2:c.3681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2703G>A
  hgvsp: ENST00000439203.1:c.2703G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3681G>A
  hgvsp: ENST00000370769.4:c.3681G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln901Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-56494217-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494217
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494217
    reference: chr 6
allele count: 2
allele frequency: 1.652783287055401e-5
allele num: 121008
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2695A>G
  hgvsp: ENSP00000431003.1:p.Lys899Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4207A>G
  hgvsp: ENSP00000359790.5:p.Lys1403Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3673A>G
  hgvsp: ENSP00000400883.2:p.Lys1225Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2695A>G
  hgvsp: ENSP00000244364.6:p.Lys899Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3673A>G
  hgvsp: ENSP00000359805.4:p.Lys1225Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3673A>G
  hgvsp: ENSP00000354508.3:p.Lys1225Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3673A>G
  hgvsp: ENSP00000307959.6:p.Lys1225Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2695A>G
  hgvsp: ENSP00000393645.2:p.Lys899Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3673A>G
  hgvsp: ENSP00000359824.2:p.Lys1225Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3793A>G
  hgvsp: ENSP00000431030.1:p.Lys1265Glu
  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.2695A>G
  hgvsp: ENSP00000359801.6:p.Lys899Glu
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2695A>G
  hgvsp: ENSP00000404924.1:p.Lys899Glu
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8514
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys899Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ

6-56494231-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494231
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494231
    reference: chr 6
allele count: 1
allele frequency: 8.334861391255063e-6
allele num: 119978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3779C>G
  hgvsp: ENSP00000431030.1:p.Ser1260Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3659C>G
  hgvsp: ENSP00000359824.2:p.Ser1220Cys
  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.2681C>G
  hgvsp: ENSP00000359801.6:p.Ser894Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2681C>G
  hgvsp: ENSP00000431003.1:p.Ser894Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2681C>G
  hgvsp: ENSP00000393645.2:p.Ser894Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4193C>G
  hgvsp: ENSP00000359790.5:p.Ser1398Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2681C>G
  hgvsp: ENSP00000244364.6:p.Ser894Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3659C>G
  hgvsp: ENSP00000354508.3:p.Ser1220Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3659C>G
  hgvsp: ENSP00000307959.6:p.Ser1220Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3659C>G
  hgvsp: ENSP00000359805.4:p.Ser1220Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3659C>G
  hgvsp: ENSP00000400883.2:p.Ser1220Cys
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2681C>G
  hgvsp: ENSP00000404924.1:p.Ser894Cys
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser894Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

6-56494261-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494261
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494261
    reference: chr 6
allele count: 3
allele frequency: 2.724053391446472e-5
allele num: 110130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2671-20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3649-20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2671-20T>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.2671-20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3649-20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3649-20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2671-20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3649-20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2671-20T>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.3649-20T>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.3769-20T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4183-20T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5613
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15614
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

6-56494269-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494269
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494269
    reference: chr 6
allele count: 7
allele frequency: 6.458398686177181e-5
allele num: 108386
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.3649-28A>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.3649-28A>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.3649-28A>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2671-28A>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.2671-28A>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2671-28A>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.4183-28A>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.3769-28A>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.2671-28A>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.2671-28A>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.3649-28A>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.3649-28A>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18797
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

6-56494275-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494275
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494275
    reference: chr 6
allele count: 3
allele frequency: 2.805311389564242e-5
allele num: 106940
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.3649-34A>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.3649-34A>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.3649-34A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2671-34A>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.3649-34A>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.3649-34A>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.3769-34A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2671-34A>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.2671-34A>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.2671-34A>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.2671-34A>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.4183-34A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19927
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

6-56494993-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56494993
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56494993
    reference: chr 6
allele count: 1
allele frequency: 8.311584686736373e-6
allele num: 120314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2670+50T>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.2670+50T>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.2670+50T>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.2670+50T>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.3648+50T>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.4182+50T>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.3648+50T>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.3648+50T>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.3768+50T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2670+50T>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.3648+50T>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.3648+50T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10028
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

6-56495001-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495001
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495001
    reference: chr 6
allele count: 257
allele frequency: 2.136006250103891e-3
allele num: 120318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3768+42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2670+42A>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.2670+42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2670+42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3648+42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3648+42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3648+42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2670+42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2670+42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3648+42A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3648+42A>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.4182+42A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29919
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12222
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 10061
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

6-56495003-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495003
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495003
    reference: chr 6
allele count: 1
allele frequency: 8.3099270388406e-6
allele num: 120338
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.2670+40C>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.2670+40C>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.3648+40C>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.2670+40C>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.4182+40C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2670+40C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2670+40C>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.3768+40C>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.3648+40C>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.3648+40C>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.3648+40C>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.3648+40C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum

6-56495009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495009
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495009
    reference: chr 6
allele count: 3
allele frequency: 2.491984117754556e-5
allele num: 120386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2670+34C>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.3648+34C>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.2670+34C>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.2670+34C>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.3648+34C>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.3648+34C>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.3768+34C>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2670+34C>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.4182+34C>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.3648+34C>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.3648+34C>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.2670+34C>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

6-56495010-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495010
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495010
    reference: chr 6
allele count: 2
allele frequency: 1.66096402351925e-5
allele num: 120412
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.2670+33T>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.2670+33T>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.2670+33T>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.3648+33T>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.4182+33T>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.3648+33T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2670+33T>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.3768+33T>C
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2670+33T>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.3648+33T>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.3648+33T>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.3648+33T>C
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10172
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-56495011-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495011
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495011
    reference: chr 6
allele count: 2
allele frequency: 1.660798511924533e-5
allele num: 120424
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.3648+32A>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.3648+32A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2670+32A>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.2670+32A>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.2670+32A>G
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2670+32A>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.2670+32A>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.4182+32A>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.3648+32A>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.3648+32A>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.3648+32A>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.3768+32A>G
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/6-56495024-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495024
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495024
    reference: chr 6
allele count: 1
allele frequency: 8.295588406085643e-6
allele num: 120546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2670+19G>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.2670+19G>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.2670+19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3648+19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2670+19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3648+19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2670+19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3648+19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4182+19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3648+19G>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.3768+19G>T
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3648+19G>T
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

6-56495036-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495036
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495036
    reference: chr 6
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3648+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2670+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2670+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3768+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2670+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3648+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4182+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3648+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2670+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2670+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3648+7G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3648+7G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2670+7G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

6-56495038-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495038
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495038
    reference: chr 6
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3648+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3648+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2670+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2670+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3648+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3768+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2670+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2670+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2670+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4182+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3648+5G>A
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3648+5G>A
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2670+5G>A
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

6-56495046-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495046
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495046
    reference: chr 6
allele count: 1
allele frequency: 8.273077750384698e-6
allele num: 120874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3645A>G
  hgvsp: ENST00000361203.3:c.3645A>G(p.%3D)
  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.2667A>G
  hgvsp: ENST00000370765.6:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2667A>G
  hgvsp: ENST00000244364.6:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2667A>G
  hgvsp: ENST00000439203.1:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3645A>G
  hgvsp: ENST00000421834.2:c.3645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3645A>G
  hgvsp: ENST00000370769.4:c.3645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2667A>G
  hgvsp: ENST00000446842.2:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2667A>G
  hgvsp: ENST00000518935.1:c.2667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3645A>G
  hgvsp: ENST00000312431.6:c.3645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3645A>G
  hgvsp: ENST00000370788.2:c.3645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3765A>G
  hgvsp: ENST00000520645.1:c.3765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4179A>G
  hgvsp: ENST00000370754.5:c.4179A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu889Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

6-56495055-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495055
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495055
    reference: chr 6
allele count: 7
allele frequency: 5.786175998941956e-5
allele num: 120978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2658A>G
  hgvsp: ENSP00000431003.1:p.Ile886Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3636A>G
  hgvsp: ENSP00000307959.6:p.Ile1212Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3636A>G
  hgvsp: ENSP00000354508.3:p.Ile1212Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3636A>G
  hgvsp: ENSP00000359824.2:p.Ile1212Met
  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.2658A>G
  hgvsp: ENSP00000359801.6:p.Ile886Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2658A>G
  hgvsp: ENSP00000393645.2:p.Ile886Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2658A>G
  hgvsp: ENSP00000404924.1:p.Ile886Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2658A>G
  hgvsp: ENSP00000244364.6:p.Ile886Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3636A>G
  hgvsp: ENSP00000359805.4:p.Ile1212Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4170A>G
  hgvsp: ENSP00000359790.5:p.Ile1390Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3636A>G
  hgvsp: ENSP00000400883.2:p.Ile1212Met
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3756A>G
  hgvsp: ENSP00000431030.1:p.Ile1252Met
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile886Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

6-56495056-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495056
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495056
    reference: chr 6
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4169T>C
  hgvsp: ENSP00000359790.5:p.Ile1390Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2657T>C
  hgvsp: ENSP00000244364.6:p.Ile886Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2657T>C
  hgvsp: ENSP00000431003.1:p.Ile886Thr
  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.2657T>C
  hgvsp: ENSP00000359801.6:p.Ile886Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3755T>C
  hgvsp: ENSP00000431030.1:p.Ile1252Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3635T>C
  hgvsp: ENSP00000400883.2:p.Ile1212Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3635T>C
  hgvsp: ENSP00000354508.3:p.Ile1212Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3635T>C
  hgvsp: ENSP00000359805.4:p.Ile1212Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3635T>C
  hgvsp: ENSP00000359824.2:p.Ile1212Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2657T>C
  hgvsp: ENSP00000393645.2:p.Ile886Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3635T>C
  hgvsp: ENSP00000307959.6:p.Ile1212Thr
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2657T>C
  hgvsp: ENSP00000404924.1:p.Ile886Thr
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile886Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

6-56495077-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495077
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495077
    reference: chr 6
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4148A>G
  hgvsp: ENSP00000359790.5:p.Lys1383Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3614A>G
  hgvsp: ENSP00000354508.3:p.Lys1205Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2636A>G
  hgvsp: ENSP00000244364.6:p.Lys879Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2636A>G
  hgvsp: ENSP00000431003.1:p.Lys879Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2636A>G
  hgvsp: ENSP00000393645.2:p.Lys879Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3734A>G
  hgvsp: ENSP00000431030.1:p.Lys1245Arg
  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.2636A>G
  hgvsp: ENSP00000359801.6:p.Lys879Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3614A>G
  hgvsp: ENSP00000307959.6:p.Lys1205Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2636A>G
  hgvsp: ENSP00000404924.1:p.Lys879Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3614A>G
  hgvsp: ENSP00000359805.4:p.Lys1205Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3614A>G
  hgvsp: ENSP00000359824.2:p.Lys1205Arg
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3614A>G
  hgvsp: ENSP00000400883.2:p.Lys1205Arg
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys879Arg
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-56495091-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495091
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495091
    reference: chr 6
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2622A>G
  hgvsp: ENST00000518935.1:c.2622A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3600A>G
  hgvsp: ENST00000370788.2:c.3600A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3600A>G
  hgvsp: ENST00000361203.3:c.3600A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2622A>G
  hgvsp: ENST00000439203.1:c.2622A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3720A>G
  hgvsp: ENST00000520645.1:c.3720A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2622A>G
  hgvsp: ENST00000244364.6:c.2622A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3600A>G
  hgvsp: ENST00000421834.2:c.3600A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3600A>G
  hgvsp: ENST00000312431.6:c.3600A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2622A>G
  hgvsp: ENST00000446842.2:c.2622A>G(p.%3D)
  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.2622A>G
  hgvsp: ENST00000370765.6:c.2622A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3600A>G
  hgvsp: ENST00000370769.4:c.3600A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4134A>G
  hgvsp: ENST00000370754.5:c.4134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala874Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

6-56495092-GCTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 56495092
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 56495089
    reference: chr 6
allele count: 4
allele frequency: 3.301583109100814e-5
allele num: 121154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000400883
  ensembl transcript: ENST00000421834
  gene symbol: DST
  hgvsc: ENST00000421834.2:c.3596_3598delAAG
  hgvsp: ENSP00000400883.2:p.Glu1199del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000244364
  ensembl transcript: ENST00000244364
  gene symbol: DST
  hgvsc: ENST00000244364.6:c.2618_2620delAAG
  hgvsp: ENSP00000244364.6:p.Glu873del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359805
  ensembl transcript: ENST00000370769
  gene symbol: DST
  hgvsc: ENST00000370769.4:c.3596_3598delAAG
  hgvsp: ENSP00000359805.4:p.Glu1199del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431003
  ensembl transcript: ENST00000518935
  gene symbol: DST
  hgvsc: ENST00000518935.1:c.2618_2620delAAG
  hgvsp: ENSP00000431003.1:p.Glu873del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359801
  ensembl transcript: ENST00000370765
  gene symbol: DST
  hgvsc: ENST00000370765.6:c.2618_2620delAAG
  hgvsp: ENSP00000359801.6:p.Glu873del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000393645
  ensembl transcript: ENST00000446842
  gene symbol: DST
  hgvsc: ENST00000446842.2:c.2618_2620delAAG
  hgvsp: ENSP00000393645.2:p.Glu873del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359790
  ensembl transcript: ENST00000370754
  gene symbol: DST
  hgvsc: ENST00000370754.5:c.4130_4132delAAG
  hgvsp: ENSP00000359790.5:p.Glu1377del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000404924
  ensembl transcript: ENST00000439203
  gene symbol: DST
  hgvsc: ENST00000439203.1:c.2618_2620delAAG
  hgvsp: ENSP00000404924.1:p.Glu873del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000307959
  ensembl transcript: ENST00000312431
  gene symbol: DST
  hgvsc: ENST00000312431.6:c.3596_3598delAAG
  hgvsp: ENSP00000307959.6:p.Glu1199del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000359824
  ensembl transcript: ENST00000370788
  gene symbol: DST
  hgvsc: ENST00000370788.2:c.3596_3598delAAG
  hgvsp: ENSP00000359824.2:p.Glu1199del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000354508
  ensembl transcript: ENST00000361203
  gene symbol: DST
  hgvsc: ENST00000361203.3:c.3596_3598delAAG
  hgvsp: ENSP00000354508.3:p.Glu1199del
  variant of: http://identifiers.org/hgnc/1090
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151914
  ensembl protein: ENSP00000431030
  ensembl transcript: ENST00000520645
  gene symbol: DST
  hgvsc: ENST00000520645.1:c.3716_3718delAAG
  hgvsp: ENSP00000431030.1:p.Glu1239del
  variant of: http://identifiers.org/hgnc/1090
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10239
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu873del
num of homozygotes: 0
reference allele: GCTT

GenotypeDepth
all individuals: 586
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 277
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 202
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4707
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10087
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 3398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9477
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3640
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49842555105713e-5
allele num: 66690
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -8.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

QD
type: SiteQuality
SIO_000300: 1.392e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

DP
type: SiteQuality
SIO_000300: 2.041777e6

FS
type: SiteQuality
SIO_000300: 1.448e0

VQSLOD
type: SiteQuality
SIO_000300: 6.07e-1

GenotypeDepth
all individuals: 277
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5980
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 482
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4699
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 10083
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9460
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3393
bin: 8.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.15e1

BaseQRankSum
type: SiteQuality
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: 2.12e-1

MQRankSum
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SIO_000300: 4.1e-2

DP
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SIO_000300: 2.04111e6

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

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

European (Finnish)
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allele frequency: 0.0e0
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Other
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African
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allele frequency: 9.620935154897056e-5
allele num: 10394
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Latino
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66648
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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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East Asian
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allele frequency: 0.0e0
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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QD
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DP
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ClippingRankSum
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SIO_000300: -3.26e-1

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

East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.002371873780286e-5
allele num: 66614
num of homozygotes: 0

South Asian
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

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

European (Finnish)
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East Asian
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African
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allele num: 10396
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Other
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MQRankSum
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QD
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DP
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 16438
num of homozygotes: 0

European (Non-Finnish)
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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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Other
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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BaseQRankSum
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

European (Finnish)
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East Asian
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European (Non-Finnish)
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South 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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MQ
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 66366
num of homozygotes: 0

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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allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.220107369448512e-4
allele num: 16392
num of homozygotes: 0

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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SIO_000300: -6.68e-1

VQSLOD
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BaseQRankSum
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SIO_000300: -7.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

DP
type: SiteQuality
SIO_000300: 1.960917e6

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 1.171e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.01504507492387e-5
allele num: 66334
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

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

BaseQRankSum
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FS
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DP
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ClippingRankSum
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SIO_000300: -9.15e-1

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509023963300537e-5
allele num: 66268
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.76e-1

MQRankSum
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ReadPosRankSum
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SIO_000300: -1.63e-1

ClippingRankSum
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DP
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InbreedingCoeff
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SIO_000300: 2.6e-3

QD
type: SiteQuality
SIO_000300: 1.496e1

FS
type: SiteQuality
SIO_000300: 4.241e0

BaseQRankSum
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SIO_000300: 3.2e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

GenotypeDepth
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 41

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2989
bin: 7.25e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.76731544800982e-5
allele num: 11406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 40
allele frequency: 2.446183953033268e-3
allele num: 16352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509160604871571e-5
allele num: 66262
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -2.688e0

QD
type: SiteQuality
SIO_000300: 1.282e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

DP
type: SiteQuality
SIO_000300: 1.902958e6

FS
type: SiteQuality
SIO_000300: 2.115e0

GenotypeDepth
all individuals: 276
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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: 2410
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 479
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.117704637220115e-5
allele num: 16346
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

ClippingRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.529e1

MQRankSum
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FS
type: SiteQuality
SIO_000300: 2.235e0

DP
type: SiteQuality
SIO_000300: 1.88103e6

GenotypeDepth
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variant carriers: 6

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.212709192335678e-4
allele num: 16492
num of homozygotes: 0

African
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allele count: 250
allele frequency: 2.405233788724264e-2
allele num: 10394
num of homozygotes: 2

Latino
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allele count: 7
allele frequency: 6.064806792583608e-4
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
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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 count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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MQ
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DP
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 618
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GenotypeQuality
all individuals: 38
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variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732801940738174e-4
allele num: 11542
num of homozygotes: 0

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

African
type: Population
allele count: 7
allele frequency: 6.73076923076923e-4
allele num: 10400
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Other
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South Asian
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European (Non-Finnish)
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allele num: 66652
num of homozygotes: 0

East Asian
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FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.62e0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

QD
type: SiteQuality
SIO_000300: 1.598e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

GenotypeDepth
all individuals: 3476
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7534
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1649
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
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GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 617
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GenotypeQuality
all individuals: 89
bin: 4.75e1
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GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 1150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7972
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000390050706592e-5
allele num: 66658
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.54e-1

QD
type: SiteQuality
SIO_000300: 1.378e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

FS
type: SiteQuality
SIO_000300: 2.057e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.00094e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.127e0

VQSLOD
type: SiteQuality
SIO_000300: 6.67e-1

GenotypeDepth
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
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variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
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GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
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: 3
allele frequency: 4.499775011249437e-5
allele num: 66670
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.001657e6

FS
type: SiteQuality
SIO_000300: 1.503e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.95e-1

QD
type: SiteQuality
SIO_000300: 1.584e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeDepth
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38825
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variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 1145
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 1652
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7528
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 880
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
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: 6606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 4.0e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 6.246e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

DP
type: SiteQuality
SIO_000300: 2.001892e6

QD
type: SiteQuality
SIO_000300: 1.506e1

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7527
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7974
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 617
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GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
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variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38877
bin: 6.25e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
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: 66660
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

QD
type: SiteQuality
SIO_000300: 9.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.25e0

MQRankSum
type: SiteQuality
SIO_000300: -8.74e-1

DP
type: SiteQuality
SIO_000300: 2.00203e6

VQSLOD
type: SiteQuality
SIO_000300: 1.91e-1

GenotypeDepth
all individuals: 292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 1147
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variant carriers: 0

GenotypeQuality
all individuals: 620
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 1700
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1653
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variant carriers: 0

GenotypeQuality
all individuals: 7527
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 876
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38967
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.498965237995261e-5
allele num: 66682
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.465e1

MQRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: -9.317e-1

DP
type: SiteQuality
SIO_000300: 2.002572e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

FS
type: SiteQuality
SIO_000300: 1.011e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1662
bin: 7.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
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
type: Population
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.00337e6

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

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 2.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

MQ
type: SiteQuality
SIO_000300: 5.905e1

GenotypeDepth
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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
all individuals: 7528
bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

African
type: Population
allele count: 8
allele frequency: 7.690828686791001e-4
allele num: 10402
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.94e-1

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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QD
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DP
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

FS
type: SiteQuality
SIO_000300: 1.652e0

MQ
type: SiteQuality
SIO_000300: 6.005e1

GenotypeDepth
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bin: 9.75e1
variant carriers: 156

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
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allele frequency: 6.048038707447727e-4
allele num: 11574
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African
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allele frequency: 2.403383964622188e-2
allele num: 10402
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InbreedingCoeff
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FS
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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: 2.5e-1

MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.496268097479092e-5
allele num: 66722
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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SIO_000300: 1.51e-1

ClippingRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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DP
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -3.0e-4

QD
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SIO_000300: 1.394e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

African
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allele count: 10
allele frequency: 9.613535858488752e-4
allele num: 10402
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: 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
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MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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SIO_000300: 1.995835e6

MQ
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SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 1.404e0

ReadPosRankSum
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SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

South Asian
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allele count: 1
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allele num: 16506
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -3.0e-4

MQRankSum
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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SIO_000300: 1.995204e6

QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6610
num of homozygotes: 0

African
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Other
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66722
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East Asian
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South Asian
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allele num: 16506
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele num: 8654
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Latino
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South Asian
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African
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European (Finnish)
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Other
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MQ
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VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 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 (Non-Finnish)
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allele count: 1
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allele num: 66726
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Latino
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East Asian
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Other
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VQSLOD
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BaseQRankSum
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SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 1.995239e6

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.998e0

FS
type: SiteQuality
SIO_000300: 1.075e0

QD
type: SiteQuality
SIO_000300: 1.209e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 188
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 315
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7317
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1714
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1671
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39310
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8026
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.48e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 8.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.007e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.614e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.91e-1

FS
type: SiteQuality
SIO_000300: 8.567e0

DP
type: SiteQuality
SIO_000300: 1.99521e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
all individuals: 268
bin: 6.75e1
variant carriers: 54

GenotypeDepth
all individuals: 8386
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1198
bin: 4.75e1
variant carriers: 12

GenotypeDepth
all individuals: 27379
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7951
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 748
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variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8003
bin: 9.75e1
variant carriers: 2825

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 16
allele frequency: 1.762114537444934e-2
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 76
allele frequency: 7.306287252451452e-3
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 133
allele frequency: 1.148730350665054e-2
allele num: 11578
num of homozygotes: 2

South Asian
type: Population
allele count: 385
allele frequency: 2.331920048455481e-2
allele num: 16510
num of homozygotes: 6

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

European (Finnish)
type: Population
allele count: 69
allele frequency: 1.043241608708799e-2
allele num: 6614
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2192
allele frequency: 3.284977820405227e-2
allele num: 66728
num of homozygotes: 35

BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.257225e6

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeDepth
all individuals: 231
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13416
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8330
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variant carriers: 0

GenotypeQuality
all individuals: 41062
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variant carriers: 0

GenotypeQuality
all individuals: 5488
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 538
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
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variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 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: 8654
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -6.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.163e0

VQSLOD
type: SiteQuality
SIO_000300: -1.689e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.16e-1

FS
type: SiteQuality
SIO_000300: 3.469e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

QD
type: SiteQuality
SIO_000300: 1.247e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.42e-1

DP
type: SiteQuality
SIO_000300: 1.933842e6

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

GenotypeDepth
all individuals: 13418
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 530
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variant carriers: 0

GenotypeDepth
all individuals: 231
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 41065
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1686
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variant carriers: 0

GenotypeQuality
all individuals: 5487
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 8327
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 794
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variant carriers: 0

GenotypeQuality
all individuals: 538
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.93395e6

QD
type: SiteQuality
SIO_000300: 1.352e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

GenotypeDepth
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 212
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variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 539
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variant carriers: 0

GenotypeQuality
all individuals: 8323
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variant carriers: 0

GenotypeQuality
all individuals: 41065
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5486
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1702
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 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: 11578
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.933961e6

QD
type: SiteQuality
SIO_000300: 1.058e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e-1

FS
type: SiteQuality
SIO_000300: 4.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.963e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeDepth
all individuals: 13418
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 820
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 212
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
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variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8326
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GenotypeQuality
all individuals: 5484
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41059
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 8.25e1
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: 11578
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
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: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.933843e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e0

QD
type: SiteQuality
SIO_000300: 1.323e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1256
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variant carriers: 0

GenotypeDepth
all individuals: 3269
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variant carriers: 0

GenotypeDepth
all individuals: 530
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41058
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5483
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1083
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8325
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
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African
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Latino
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East Asian
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South Asian
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FS
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BaseQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 16510
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Other
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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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Latino
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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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QD
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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Other
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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East Asian
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African
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European (Finnish)
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South Asian
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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African
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East Asian
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South Asian
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VQSLOD
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FS
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QD
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DP
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Non-Finnish)
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African
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Latino
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FS
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BaseQRankSum
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DP
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MQ
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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Latino
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South Asian
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African
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East Asian
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European (Non-Finnish)
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VQSLOD
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FS
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DP
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

South Asian
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allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

East 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 frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
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VQSLOD
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QD
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MQ
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SIO_000300: 5.963e1

BaseQRankSum
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SIO_000300: 1.03e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10398
num of homozygotes: 0

South Asian
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allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

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

European (Non-Finnish)
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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
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num of homozygotes: 0

Latino
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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MQ
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DP
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QD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 3

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 6.820809248554913e-3
allele num: 8650
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: 2.423654871546292e-4
allele num: 16504
num of homozygotes: 0

European (Finnish)
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allele count: 0
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num of homozygotes: 0

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

MQ
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SIO_000300: 5.973e1

ClippingRankSum
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QD
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FS
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DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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SIO_000300: 2.52e-1

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10390
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

VQSLOD
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SIO_000300: 1.07e0

DP
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SIO_000300: 1.928258e6

BaseQRankSum
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MQRankSum
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SIO_000300: -3.7e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
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SIO_000300: 5.963e1

QD
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FS
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SIO_000300: 2.019e0

ClippingRankSum
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SIO_000300: -1.317e0

ReadPosRankSum
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SIO_000300: 1.1e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
allele frequency: 3.006885768409658e-5
allele num: 66514
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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European (Finnish)
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Other
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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MQ
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65874
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Other
type: Population
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Latino
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East Asian
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South Asian
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QD
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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FS
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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African
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Other
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Latino
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East Asian
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South Asian
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DP
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10442
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.198219787743923e-4
allele num: 58420
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9238
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 7.93e-1

MQRankSum
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InbreedingCoeff
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SIO_000300: -3.8e-3

FS
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SIO_000300: 2.899e0

QD
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BaseQRankSum
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SIO_000300: 2.45e0

ClippingRankSum
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SIO_000300: -4.24e-1

DP
type: SiteQuality
SIO_000300: 1.419907e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9116
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 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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 5.222841225626741e-5
allele num: 57440
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.833e1

DP
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SIO_000300: 1.360171e6

BaseQRankSum
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SIO_000300: -3.163e0

VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.122e0

InbreedingCoeff
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SIO_000300: -4.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

QD
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SIO_000300: 1.305e1

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele 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: 1.508386629660915e-5
allele num: 66296
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 4.48e0

InbreedingCoeff
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SIO_000300: 6.2e-3

MQRankSum
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SIO_000300: 1.41e0

FS
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QD
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VQSLOD
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SIO_000300: -1.496e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

DP
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SIO_000300: 1.756142e6

GenotypeDepth
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variant carriers: 15

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 256

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 328
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.112469437652811e-5
allele num: 16360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 63
allele frequency: 9.545454545454546e-3
allele num: 6600
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.990445859872612e-4
allele num: 10048
num of homozygotes: 0

European (Non-Finnish)
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allele count: 184
allele frequency: 2.775431398576083e-3
allele num: 66296
num of homozygotes: 1

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

Other
type: Population
allele count: 7
allele frequency: 7.760532150776054e-3
allele num: 902
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

DP
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SIO_000300: 1.762409e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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BaseQRankSum
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SIO_000300: 4.56e0

ClippingRankSum
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SIO_000300: -1.19e-1

QD
type: SiteQuality
SIO_000300: 1.544e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1365
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 336
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.942334460131238e-5
allele num: 10058
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66302
num of homozygotes: 0

Other
type: Population
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MQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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DP
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MQ
type: SiteQuality
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BaseQRankSum
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

Other
type: Population
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 3.029385034837928e-4
allele num: 6602
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.940357852882704e-5
allele num: 10060
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Latino
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InbreedingCoeff
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MQRankSum
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FS
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QD
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VQSLOD
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MQ
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 5.29e-1

ClippingRankSum
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DP
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
all individuals: 1929
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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African
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European (Non-Finnish)
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allele num: 66332
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DP
type: SiteQuality
SIO_000300: 1.759686e6

BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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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
all individuals: 236
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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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European (Finnish)
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European (Non-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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MQ
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BaseQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Other
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.076072426783327e-5
allele num: 16458
num of homozygotes: 0

Latino
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African
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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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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6606
num of homozygotes: 0

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

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41294
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1938
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4219
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 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: 10316
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.351e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.773064e6

VQSLOD
type: SiteQuality
SIO_000300: 6.6e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

QD
type: SiteQuality
SIO_000300: 1.725e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

GenotypeDepth
all individuals: 290
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 672
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1938
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41325
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4216
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8020
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.773315e6

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

QD
type: SiteQuality
SIO_000300: 1.2e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
SIO_000300: 3.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.991e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.343e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

GenotypeDepth
all individuals: 53
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1009
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2172
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1398
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 41342
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8010
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4217
bin: 9.75e1
variant carriers: 4