20-35390967-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35390967
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35390967
    reference: chr 20
allele count: 1
allele frequency: 9.094050672050345e-6
allele num: 109962
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.503-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.455-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.287-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.886-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.503-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.182-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.203-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.503-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.504-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.503-16A>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.514-16A>C
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

20-35390971-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35390971
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35390971
    reference: chr 20
allele count: 5
allele frequency: 4.609824457884644e-5
allele num: 108464
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.503-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.514-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.503-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.182-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.287-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.203-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.504-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.503-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.455-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.503-20C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.886-20C>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21150
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1821
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

20-35390972-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35390972
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35390972
    reference: chr 20
allele count: 1
allele frequency: 9.267840593141798e-6
allele num: 107900
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.182-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.504-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.455-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.886-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.287-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.503-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.503-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.203-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.503-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.514-21A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.503-21A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24979
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ

20-35390993-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35390993
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35390993
    reference: chr 20
allele count: 3
allele frequency: 3.147491449314896e-5
allele num: 95314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.287-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.203-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.182-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.503-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.503-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.504-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.455-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.503-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.503-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.886-42A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.514-42A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22957
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13743
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

20-35390995-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35390995
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35390995
    reference: chr 20
allele count: 0
allele frequency: 0.0e0
allele num: 94770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.182-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.503-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.503-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.504-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.503-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.455-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.514-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.503-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.287-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.886-44G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.203-44G>C
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18247
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

20-35390996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35390996
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35390996
    reference: chr 20
allele count: 6
allele frequency: 6.474028356244201e-5
allele num: 92678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.886-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.503-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.182-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.503-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.203-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.503-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.504-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.503-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.287-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.455-45C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.514-45C>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5902
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13377
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6047
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

20-35391000-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35391000
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35391000
    reference: chr 20
allele count: 12
allele frequency: 1.332889036987671e-4
allele num: 90030
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.514-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.455-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.504-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.503-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.503-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.886-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.503-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.287-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.203-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.503-49A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.182-49A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21479
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12982
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13134
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

20-35395130-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395130
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395130
    reference: chr 20
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.454+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.202+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.885+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.503+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.513+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.502+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.286+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.502+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.502+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.502+42C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.181+42C>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20973
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

20-35395137-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395137
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395137
    reference: chr 20
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.502+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.286+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.502+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.885+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.513+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.202+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.454+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.181+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.502+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.502+35G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.503+35G>C
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

20-35395158-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395158
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395158
    reference: chr 20
allele count: 3
allele frequency: 2.472310126582278e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.454+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.503+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.513+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.502+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.502+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.181+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.502+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.885+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.202+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.502+14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.286+14A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2720
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

20-35395161-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395161
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395161
    reference: chr 20
allele count: 7
allele frequency: 5.768723628691983e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.503+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.202+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.513+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.502+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.181+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.502+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.454+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.885+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.502+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.286+11A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.502+11A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6498
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

20-35395174-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395174
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395174
    reference: chr 20
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.200A>T
  hgvsp: ENSP00000395760.1:p.Lys67Ile
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.179A>T
  hgvsp: ENSP00000362839.4:p.Lys60Ile
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.452A>T
  hgvsp: ENSP00000404463.1:p.Lys151Ile
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.500A>T
  hgvsp: ENSP00000362850.3:p.Lys167Ile
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.500A>T
  hgvsp: ENSP00000399654.1:p.Lys167Ile
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.284A>T
  hgvsp: ENSP00000362845.3:p.Lys95Ile
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.883A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.501A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.500A>T
  hgvsp: ENSP00000362855.4:p.Lys167Ile
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.511A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.500A>T
  hgvsp: ENSP00000389810.1:p.Lys167Ile
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys167Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

20-35395190-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395190
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395190
    reference: chr 20
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.184G>A
  hgvsp: ENSP00000395760.1:p.Glu62Lys
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.484G>A
  hgvsp: ENSP00000399654.1:p.Glu162Lys
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.268G>A
  hgvsp: ENSP00000362845.3:p.Glu90Lys
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.484G>A
  hgvsp: ENSP00000389810.1:p.Glu162Lys
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.484G>A
  hgvsp: ENSP00000362855.4:p.Glu162Lys
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.495G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.163G>A
  hgvsp: ENSP00000362839.4:p.Glu55Lys
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.867G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.484G>A
  hgvsp: ENSP00000362850.3:p.Glu162Lys
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.436G>A
  hgvsp: ENSP00000404463.1:p.Glu146Lys
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.485G>A
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu162Lys
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

20-35395201-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395201
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395201
    reference: chr 20
allele count: 4
allele frequency: 3.297826732183491e-5
allele num: 121292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.152G>A
  hgvsp: ENSP00000362839.4:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.856G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.473G>A
  hgvsp: ENSP00000389810.1:p.Gly158Asp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.425G>A
  hgvsp: ENSP00000404463.1:p.Gly142Asp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.474G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.257G>A
  hgvsp: ENSP00000362845.3:p.Gly86Asp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.473G>A
  hgvsp: ENSP00000399654.1:p.Gly158Asp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.173G>A
  hgvsp: ENSP00000395760.1:p.Gly58Asp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.473G>A
  hgvsp: ENSP00000362850.3:p.Gly158Asp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.484G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.473G>A
  hgvsp: ENSP00000362855.4:p.Gly158Asp
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly158Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

20-35395205-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395205
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395206
    reference: chr 20
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.468dupT
  hgvsp: ENSP00000399654.1:p.Lys157Ter
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.468dupT
  hgvsp: ENSP00000362850.3:p.Lys157Ter
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.468dupT
  hgvsp: ENSP00000389810.1:p.Lys157Ter
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.420dupT
  hgvsp: ENSP00000404463.1:p.Lys141Ter
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.168dupT
  hgvsp: ENSP00000395760.1:p.Lys57Ter
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.252dupT
  hgvsp: ENSP00000362845.3:p.Lys85Ter
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.851dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.479dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.147dupT
  hgvsp: ENSP00000362839.4:p.Lys50Ter
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.468dupT
  hgvsp: ENSP00000362855.4:p.Lys157Ter
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.469dupT
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys157Ter
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

20-35395208-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395208
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395208
    reference: chr 20
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.466A>G
  hgvsp: ENSP00000389810.1:p.Thr156Ala
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.166A>G
  hgvsp: ENSP00000395760.1:p.Thr56Ala
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.145A>G
  hgvsp: ENSP00000362839.4:p.Thr49Ala
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.466A>G
  hgvsp: ENSP00000362850.3:p.Thr156Ala
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.418A>G
  hgvsp: ENSP00000404463.1:p.Thr140Ala
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.250A>G
  hgvsp: ENSP00000362845.3:p.Thr84Ala
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.477A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.466A>G
  hgvsp: ENSP00000399654.1:p.Thr156Ala
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.467A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.849A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.466A>G
  hgvsp: ENSP00000362855.4:p.Thr156Ala
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr156Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

20-35395223-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395223
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395223
    reference: chr 20
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.451C>T
  hgvsp: ENSP00000362850.3:p.Pro151Ser
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.403C>T
  hgvsp: ENSP00000404463.1:p.Pro135Ser
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.834C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.235C>T
  hgvsp: ENSP00000362845.3:p.Pro79Ser
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.451C>T
  hgvsp: ENSP00000389810.1:p.Pro151Ser
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.130C>T
  hgvsp: ENSP00000362839.4:p.Pro44Ser
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.452C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.151C>T
  hgvsp: ENSP00000395760.1:p.Pro51Ser
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.451C>T
  hgvsp: ENSP00000399654.1:p.Pro151Ser
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.462C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.451C>T
  hgvsp: ENSP00000362855.4:p.Pro151Ser
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro151Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

20-35395223-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395223
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395223
    reference: chr 20
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.451C>A
  hgvsp: ENSP00000362855.4:p.Pro151Thr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.452C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.130C>A
  hgvsp: ENSP00000362839.4:p.Pro44Thr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.151C>A
  hgvsp: ENSP00000395760.1:p.Pro51Thr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.451C>A
  hgvsp: ENSP00000362850.3:p.Pro151Thr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.403C>A
  hgvsp: ENSP00000404463.1:p.Pro135Thr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.451C>A
  hgvsp: ENSP00000399654.1:p.Pro151Thr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.462C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.451C>A
  hgvsp: ENSP00000389810.1:p.Pro151Thr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.235C>A
  hgvsp: ENSP00000362845.3:p.Pro79Thr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.834C>A
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro151Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/20-35395227-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395227
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395227
    reference: chr 20
allele count: 3
allele frequency: 2.475533477464394e-5
allele num: 121186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.399T>G
  hgvsp: ENST00000448110.2:c.399T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.126T>G
  hgvsp: ENST00000373734.4:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.447T>G
  hgvsp: ENST00000426836.1:c.447T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.447T>G
  hgvsp: ENST00000373750.4:c.447T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.231T>G
  hgvsp: ENST00000373740.3:c.231T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.447T>G
  hgvsp: ENST00000447406.1:c.447T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.147T>G
  hgvsp: ENST00000438549.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.448T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.447T>G
  hgvsp: ENST00000373745.3:c.447T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.830T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.458T>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu149Leu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

20-35395229-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395229
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395229
    reference: chr 20
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.145C>G
  hgvsp: ENSP00000395760.1:p.Leu49Val
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.445C>G
  hgvsp: ENSP00000362850.3:p.Leu149Val
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.124C>G
  hgvsp: ENSP00000362839.4:p.Leu42Val
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.229C>G
  hgvsp: ENSP00000362845.3:p.Leu77Val
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.397C>G
  hgvsp: ENSP00000404463.1:p.Leu133Val
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.445C>G
  hgvsp: ENSP00000399654.1:p.Leu149Val
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.446C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.456C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.828C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.445C>G
  hgvsp: ENSP00000389810.1:p.Leu149Val
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.445C>G
  hgvsp: ENSP00000362855.4:p.Leu149Val
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu149Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

20-35395232-TCTGAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395232
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395227
    reference: chr 20
allele count: 15
allele frequency: 1.23807322790452e-4
allele num: 121156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.438_442delTTCAG
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.820_824delTTCAG
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.389_393delTTCAG
  hgvsp: ENSP00000404463.1:p.Ile130LysfsTer3
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.448_452delTTCAG
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.437_441delTTCAG
  hgvsp: ENSP00000362855.4:p.Ile146LysfsTer3
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.221_225delTTCAG
  hgvsp: ENSP00000362845.3:p.Ile74LysfsTer3
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.137_141delTTCAG
  hgvsp: ENSP00000395760.1:p.Ile46LysfsTer3
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.437_441delTTCAG
  hgvsp: ENSP00000399654.1:p.Ile146LysfsTer3
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.116_120delTTCAG
  hgvsp: ENSP00000362839.4:p.Ile39LysfsTer3
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.437_441delTTCAG
  hgvsp: ENSP00000389810.1:p.Ile146LysfsTer3
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.437_441delTTCAG
  hgvsp: ENSP00000362850.3:p.Ile146LysfsTer3
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 12778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile146LysfsTer3
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: TCTGAA
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

20-35395245-CTAAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395245
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395241
    reference: chr 20
allele count: 2
allele frequency: 1.653165812530997e-5
allele num: 120980
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.430-5_430-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.382-5_382-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.431-5_431-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.441-5_441-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.813-5_813-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.430-5_430-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.130-5_130-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.109-5_109-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.214-5_214-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.430-5_430-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.430-5_430-2delTTTA
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.430-5_430-2delTTTA
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: CTAAA
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

20-35395250-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395250
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395250
    reference: chr 20
allele count: 2
allele frequency: 1.654341820106871e-5
allele num: 120894
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.431-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.430-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.214-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.130-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.430-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.382-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.109-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.813-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.441-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.430-6A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.430-6A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7210
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.430-6A>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

20-35395251-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395251
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395251
    reference: chr 20
allele count: 1
allele frequency: 8.274583788435442e-6
allele num: 120852
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.109-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.430-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.430-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.813-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.430-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.430-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.130-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.214-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.441-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.431-7T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.382-7T>C
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.430-7T>C
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

20-35395254-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395254
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395255
    reference: chr 20
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.382-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.441-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.431-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.214-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.430-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.430-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.430-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.813-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.109-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.130-11dupT
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.430-11dupT
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3537
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

20-35395254-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395254
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395254
    reference: chr 20
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.109-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.431-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.430-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.430-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.130-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.441-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.430-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.813-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.430-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.382-10C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.214-10C>A
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3537
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/20-35395256-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395256
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395256
    reference: chr 20
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.430-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.382-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.109-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.214-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.430-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.431-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.130-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.430-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.430-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.441-12T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.813-12T>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7206
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

20-35395269-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395269
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395269
    reference: chr 20
allele count: 1
allele frequency: 8.320021299254527e-6
allele num: 120192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.130-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.430-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.430-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.431-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.813-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.430-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.214-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.441-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.430-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.382-25A>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.109-25A>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8603
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

20-35395270-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395270
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395270
    reference: chr 20
allele count: 3
allele frequency: 2.497169874142639e-5
allele num: 120136
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.430-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.130-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.441-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.813-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.382-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.430-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.430-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.430-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.214-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.431-26T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.109-26T>A
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

20-35395290-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35395290
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35395290
    reference: chr 20
allele count: 1
allele frequency: 8.396869646995599e-6
allele num: 119092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.441-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.431-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.382-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.430-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.130-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.813-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.430-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.430-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.430-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.109-46C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.214-46C>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8124
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/20-35396322-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396322
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396322
    reference: chr 20
allele count: 2
allele frequency: 1.651718613217052e-5
allele num: 121086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+50G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+50G>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

20-35396325-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396325
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396325
    reference: chr 20
allele count: 1
allele frequency: 8.256138438929344e-6
allele num: 121122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+47A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+47A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7853
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

20-35396326-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396326
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396326
    reference: chr 20
allele count: 2
allele frequency: 1.651173158529135e-5
allele num: 121126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+46T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+46T>C
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/20-35396328-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396328
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396328
    reference: chr 20
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+44G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+44G>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5218
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

20-35396329-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396329
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396329
    reference: chr 20
allele count: 1
allele frequency: 8.255184255712587e-6
allele num: 121136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+43T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+43T>C
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/20-35396337-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396337
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396337
    reference: chr 20
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+35T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+35T>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

20-35396339-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396339
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396339
    reference: chr 20
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+33G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+33G>A
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12442
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

20-35396353-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396353
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396353
    reference: chr 20
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+19G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+19G>A
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/20-35396359-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396359
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396359
    reference: chr 20
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+13T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+13T>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

20-35396359-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396359
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396359
    reference: chr 20
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+13T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+13T>A
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

20-35396362-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396362
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396362
    reference: chr 20
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.429+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.381+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.429+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.429+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.430+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.108+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.129+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.812+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.440+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.213+10T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.429+10T>A
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

20-35396374-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396374
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396374
    reference: chr 20
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.427C>G
  hgvsp: ENSP00000399654.1:p.Gln143Glu
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.106C>G
  hgvsp: ENSP00000362839.4:p.Gln36Glu
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.428C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.427C>G
  hgvsp: ENSP00000389810.1:p.Gln143Glu
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.379C>G
  hgvsp: ENSP00000404463.1:p.Gln127Glu
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.438C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.427C>G
  hgvsp: ENSP00000362855.4:p.Gln143Glu
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.427C>G
  hgvsp: ENSP00000362850.3:p.Gln143Glu
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.810C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.127C>G
  hgvsp: ENSP00000395760.1:p.Gln43Glu
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.211C>G
  hgvsp: ENSP00000362845.3:p.Gln71Glu
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln143Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

20-35396376-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396376
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396376
    reference: chr 20
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.425T>A
  hgvsp: ENSP00000399654.1:p.Phe142Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.808T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.425T>A
  hgvsp: ENSP00000389810.1:p.Phe142Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.426T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.209T>A
  hgvsp: ENSP00000362845.3:p.Phe70Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.125T>A
  hgvsp: ENSP00000395760.1:p.Phe42Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.425T>A
  hgvsp: ENSP00000362850.3:p.Phe142Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.425T>A
  hgvsp: ENSP00000362855.4:p.Phe142Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.104T>A
  hgvsp: ENSP00000362839.4:p.Phe35Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.436T>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.377T>A
  hgvsp: ENSP00000404463.1:p.Phe126Tyr
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8605
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe142Tyr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

20-35396380-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396380
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396380
    reference: chr 20
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.205A>G
  hgvsp: ENSP00000362845.3:p.Ser69Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.421A>G
  hgvsp: ENSP00000362855.4:p.Ser141Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.421A>G
  hgvsp: ENSP00000362850.3:p.Ser141Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.100A>G
  hgvsp: ENSP00000362839.4:p.Ser34Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.421A>G
  hgvsp: ENSP00000389810.1:p.Ser141Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.421A>G
  hgvsp: ENSP00000399654.1:p.Ser141Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.432A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.121A>G
  hgvsp: ENSP00000395760.1:p.Ser41Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.373A>G
  hgvsp: ENSP00000404463.1:p.Ser125Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.804A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.422A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser141Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

20-35396403-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396403
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396403
    reference: chr 20
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.398G>A
  hgvsp: ENSP00000399654.1:p.Arg133Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.398G>A
  hgvsp: ENSP00000389810.1:p.Arg133Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.398G>A
  hgvsp: ENSP00000362850.3:p.Arg133Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.77G>A
  hgvsp: ENSP00000362839.4:p.Arg26Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.409G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.98G>A
  hgvsp: ENSP00000395760.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.399G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.182G>A
  hgvsp: ENSP00000362845.3:p.Arg61Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.350G>A
  hgvsp: ENSP00000404463.1:p.Arg117Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.781G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.398G>A
  hgvsp: ENSP00000362855.4:p.Arg133Gln
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg133Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

20-35396404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396404
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396404
    reference: chr 20
allele count: 3
allele frequency: 2.474430880897394e-5
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.780C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.397C>T
  hgvsp: ENSP00000399654.1:p.Arg133Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.408C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.398C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.397C>T
  hgvsp: ENSP00000362850.3:p.Arg133Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.397C>T
  hgvsp: ENSP00000362855.4:p.Arg133Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.397C>T
  hgvsp: ENSP00000389810.1:p.Arg133Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.76C>T
  hgvsp: ENSP00000362839.4:p.Arg26Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.97C>T
  hgvsp: ENSP00000395760.1:p.Arg33Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.349C>T
  hgvsp: ENSP00000404463.1:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.181C>T
  hgvsp: ENSP00000362845.3:p.Arg61Trp
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg133Trp
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: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

20-35396423-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396423
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396423
    reference: chr 20
allele count: 8
allele frequency: 6.597829314155642e-5
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.378C>T
  hgvsp: ENST00000426836.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.57C>T
  hgvsp: ENST00000373734.4:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.379C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.378C>T
  hgvsp: ENST00000373745.3:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.378C>T
  hgvsp: ENST00000447406.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.389C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.330C>T
  hgvsp: ENST00000448110.2:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.378C>T
  hgvsp: ENST00000373750.4:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.78C>T
  hgvsp: ENST00000438549.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.162C>T
  hgvsp: ENST00000373740.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.761C>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val126Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

20-35396428-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396428
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396428
    reference: chr 20
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.373A>G
  hgvsp: ENSP00000389810.1:p.Ser125Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.373A>G
  hgvsp: ENSP00000362855.4:p.Ser125Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.373A>G
  hgvsp: ENSP00000362850.3:p.Ser125Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.52A>G
  hgvsp: ENSP00000362839.4:p.Ser18Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.384A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.373A>G
  hgvsp: ENSP00000399654.1:p.Ser125Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.756A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.157A>G
  hgvsp: ENSP00000362845.3:p.Ser53Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.73A>G
  hgvsp: ENSP00000395760.1:p.Ser25Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.374A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.325A>G
  hgvsp: ENSP00000404463.1:p.Ser109Gly
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser125Gly
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

20-35396436-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396436
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396436
    reference: chr 20
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.44G>C
  hgvsp: ENSP00000362839.4:p.Arg15Pro
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.365G>C
  hgvsp: ENSP00000362855.4:p.Arg122Pro
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.366G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.149G>C
  hgvsp: ENSP00000362845.3:p.Arg50Pro
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.376G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.317G>C
  hgvsp: ENSP00000404463.1:p.Arg106Pro
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.365G>C
  hgvsp: ENSP00000389810.1:p.Arg122Pro
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.365G>C
  hgvsp: ENSP00000362850.3:p.Arg122Pro
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.365G>C
  hgvsp: ENSP00000399654.1:p.Arg122Pro
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.748G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.65G>C
  hgvsp: ENSP00000395760.1:p.Arg22Pro
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg122Pro
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

20-35396436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396436
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396436
    reference: chr 20
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.366G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.748G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.44G>A
  hgvsp: ENSP00000362839.4:p.Arg15Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.65G>A
  hgvsp: ENSP00000395760.1:p.Arg22Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.149G>A
  hgvsp: ENSP00000362845.3:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.365G>A
  hgvsp: ENSP00000399654.1:p.Arg122Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.376G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.365G>A
  hgvsp: ENSP00000362850.3:p.Arg122Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.365G>A
  hgvsp: ENSP00000389810.1:p.Arg122Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.317G>A
  hgvsp: ENSP00000404463.1:p.Arg106Gln
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.365G>A
  hgvsp: ENSP00000362855.4:p.Arg122Gln
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg122Gln
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

20-35396437-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396437
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396437
    reference: chr 20
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.316C>A
  hgvsp: ENST00000448110.2:c.316C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.43C>A
  hgvsp: ENST00000373734.4:c.43C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.365C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.364C>A
  hgvsp: ENST00000447406.1:c.364C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.747C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.148C>A
  hgvsp: ENST00000373740.3:c.148C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.375C>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.364C>A
  hgvsp: ENST00000373750.4:c.364C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.64C>A
  hgvsp: ENST00000438549.1:c.64C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.364C>A
  hgvsp: ENST00000426836.1:c.364C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.364C>A
  hgvsp: ENST00000373745.3:c.364C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg122Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

20-35396437-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396437
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396437
    reference: chr 20
allele count: 4
allele frequency: 3.299567756623883e-5
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.364C>T
  hgvsp: ENSP00000362850.3:p.Arg122Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.43C>T
  hgvsp: ENSP00000362839.4:p.Arg15Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.64C>T
  hgvsp: ENSP00000395760.1:p.Arg22Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.375C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.747C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.364C>T
  hgvsp: ENSP00000399654.1:p.Arg122Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.364C>T
  hgvsp: ENSP00000362855.4:p.Arg122Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.364C>T
  hgvsp: ENSP00000389810.1:p.Arg122Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.148C>T
  hgvsp: ENSP00000362845.3:p.Arg50Trp
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.365C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.316C>T
  hgvsp: ENSP00000404463.1:p.Arg106Trp
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg122Trp
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

20-35396440-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396440
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396440
    reference: chr 20
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.361A>G
  hgvsp: ENSP00000362850.3:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.372A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.361A>G
  hgvsp: ENSP00000399654.1:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.313A>G
  hgvsp: ENSP00000404463.1:p.Ser105Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.361A>G
  hgvsp: ENSP00000389810.1:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.40A>G
  hgvsp: ENSP00000362839.4:p.Ser14Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.61A>G
  hgvsp: ENSP00000395760.1:p.Ser21Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.361A>G
  hgvsp: ENSP00000362855.4:p.Ser121Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.145A>G
  hgvsp: ENSP00000362845.3:p.Ser49Gly
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.362A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.744A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser121Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

20-35396443-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396443
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396443
    reference: chr 20
allele count: 2
allele frequency: 1.649811096629436e-5
allele num: 121226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.369C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.358C>T
  hgvsp: ENSP00000362850.3:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.358C>T
  hgvsp: ENSP00000389810.1:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.359C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.358C>T
  hgvsp: ENSP00000399654.1:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.358C>T
  hgvsp: ENSP00000362855.4:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.310C>T
  hgvsp: ENSP00000404463.1:p.Leu104Phe
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.37C>T
  hgvsp: ENSP00000362839.4:p.Leu13Phe
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.741C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.142C>T
  hgvsp: ENSP00000362845.3:p.Leu48Phe
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.58C>T
  hgvsp: ENSP00000395760.1:p.Leu20Phe
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu120Phe
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

20-35396446-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396446
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396446
    reference: chr 20
allele count: 2
allele frequency: 1.649783878311941e-5
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-1G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-1G>C
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
hgvs: c.356-1G>C
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

20-35396448-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396448
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396448
    reference: chr 20
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-3T>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-3T>C
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.356-3T>C
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/20-35396449-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396449
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396449
    reference: chr 20
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-4T>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-4T>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.356-4T>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/20-35396450-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396450
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396450
    reference: chr 20
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-5G>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-5G>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.356-5G>T
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

20-35396459-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396459
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396459
    reference: chr 20
allele count: 78
allele frequency: 6.435962176345363e-4
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-14A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-14A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10941
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 12441
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

20-35396473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396473
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396473
    reference: chr 20
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-28C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-28C>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8603
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

20-35396479-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396479
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396479
    reference: chr 20
allele count: 56
allele frequency: 4.622521585524904e-4
allele num: 121146
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-34C>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-34C>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10897
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6172
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 12247
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5208
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

20-35396479-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396479
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396479
    reference: chr 20
allele count: 2
allele frequency: 1.650900566258894e-5
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-34C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-34C>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6172
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12247
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

20-35396481-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396481
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396481
    reference: chr 20
allele count: 1
allele frequency: 8.256411103221652e-6
allele num: 121118
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-36A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-36A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11560
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD

20-35396489-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35396489
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35396489
    reference: chr 20
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.357-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.140-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.35-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.367-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.356-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.56-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.356-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.739-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.356-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.308-44A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.356-44A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10567
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

20-35399249-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35399249
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35399249
    reference: chr 20
allele count: 1
allele frequency: 8.859907148173087e-6
allele num: 112868
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.355+27G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.366+27G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.139+27G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.356+2548G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.55+27G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.34+579G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.355+27G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.355+27G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.355+27G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.738+27G>A
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.307+27G>A
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2765
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

20-35399254-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35399254
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35399254
    reference: chr 20
allele count: 1
allele frequency: 8.828462964597864e-6
allele num: 113270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.355+22A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.139+22A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.738+22A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.366+22A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.55+22A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.307+22A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.355+22A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.355+22A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.356+2543A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.34+574A>G
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.355+22A>G
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

20-35399268-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35399268
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35399268
    reference: chr 20
allele count: 1
allele frequency: 8.704583833846904e-6
allele num: 114882
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.34+560G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.355+8G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.355+8G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.55+8G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.366+8G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.307+8G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.355+8G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.356+2529G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.355+8G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.738+8G>C
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.139+8G>C
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.355+8G>C
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

20-35399291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 35399291
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 35399291
    reference: chr 20
allele count: 2
allele frequency: 1.677345768056627e-5
allele num: 119236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000399654
  ensembl transcript: ENST00000447406
  gene symbol: DSN1
  hgvsc: ENST00000447406.1:c.340C>T
  hgvsp: ENSP00000399654.1:p.His114Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000404463
  ensembl transcript: ENST00000448110
  gene symbol: DSN1
  hgvsc: ENST00000448110.2:c.292C>T
  hgvsp: ENSP00000404463.1:p.His98Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000480153
  gene symbol: DSN1
  hgvsc: ENST00000480153.1:n.723C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362845
  ensembl transcript: ENST00000373740
  gene symbol: DSN1
  hgvsc: ENST00000373740.3:c.124C>T
  hgvsp: ENSP00000362845.3:p.His42Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362839
  ensembl transcript: ENST00000373734
  gene symbol: DSN1
  hgvsc: ENST00000373734.4:c.34+537C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000395760
  ensembl transcript: ENST00000438549
  gene symbol: DSN1
  hgvsc: ENST00000438549.1:c.40C>T
  hgvsp: ENSP00000395760.1:p.His14Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362850
  ensembl transcript: ENST00000373745
  gene symbol: DSN1
  hgvsc: ENST00000373745.3:c.340C>T
  hgvsp: ENSP00000362850.3:p.His114Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000362855
  ensembl transcript: ENST00000373750
  gene symbol: DSN1
  hgvsc: ENST00000373750.4:c.340C>T
  hgvsp: ENSP00000362855.4:p.His114Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000473615
  gene symbol: DSN1
  hgvsc: ENST00000473615.1:n.351C>T
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000149636
  ensembl protein: ENSP00000389810
  ensembl transcript: ENST00000426836
  gene symbol: DSN1
  hgvsc: ENST00000426836.1:c.340C>T
  hgvsp: ENSP00000389810.1:p.His114Tyr
  variant of: http://identifiers.org/hgnc/16165
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000149636
  ensembl transcript: ENST00000492703
  gene symbol: DSN1
  hgvsc: ENST00000492703.1:n.356+2506C>T
  variant of: http://identifiers.org/hgnc/16165
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His114Tyr
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 15113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31772
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2548
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2755
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 461
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59790
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.597176408497163e-5
allele num: 15158
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10638
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.749e1

MQ
type: SiteQuality
SIO_000300: 5.834e1

MQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

FS
type: SiteQuality
SIO_000300: 2.026e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.706e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.837e0

DP
type: SiteQuality
SIO_000300: 1.26441e6

GenotypeQuality
all individuals: 3467
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 292
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2212
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27846
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17393
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3287
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7818
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 3.240440699935191e-4
allele num: 9258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.39662375598655e-5
allele num: 58882
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10480
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.223e0

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

QD
type: SiteQuality
SIO_000300: 1.203e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.939e0

DP
type: SiteQuality
SIO_000300: 1.2182e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3856
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3943
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18536
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 258
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10422
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.707591953826714e-5
allele num: 58562
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.462e0

MQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

DP
type: SiteQuality
SIO_000300: 1.188813e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.52e-1

FS
type: SiteQuality
SIO_000300: 2.884e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e-1

QD
type: SiteQuality
SIO_000300: 1.497e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 730
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2071
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8961
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17839
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4457
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2635
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2844
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6366
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 9.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.967419532541119e-5
allele num: 50828
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.465845793022574e-4
allele num: 6822
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.380073800738008e-5
allele num: 13550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.509e0

DP
type: SiteQuality
SIO_000300: 9.70426e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.66e-1

QD
type: SiteQuality
SIO_000300: 1.167e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

GenotypeQuality
all individuals: 367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8835
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2468
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6084
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6288
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4786
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2051
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2687
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2144
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2058
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8262
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6762
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50572
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 9.303000000000001e0

DP
type: SiteQuality
SIO_000300: 9.68834e5

MQ
type: SiteQuality
SIO_000300: 5.684e1

QD
type: SiteQuality
SIO_000300: 1.157e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.657e-1

GenotypeQuality
all individuals: 2553
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2781
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16916
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6393
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3463
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3725
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 8894
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2172
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8138
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.027492802400551e-5
allele num: 49322
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.766194636938837e-4
allele num: 13276
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5682
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.934e0

DP
type: SiteQuality
SIO_000300: 9.60099e5

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 131
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7942
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47814
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8658
num of homozygotes: 0

South Asian
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allele count: 12
allele frequency: 9.295120061967467e-4
allele num: 12910
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5596
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

VQSLOD
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SIO_000300: 1.27e0

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -6.6e-1

InbreedingCoeff
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SIO_000300: -8.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

FS
type: SiteQuality
SIO_000300: 3.026e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

QD
type: SiteQuality
SIO_000300: 1.218e1

DP
type: SiteQuality
SIO_000300: 9.52423e5

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.99e0

QD
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SIO_000300: 1.792e1

MQRankSum
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SIO_000300: 1.74e0

ReadPosRankSum
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SIO_000300: 1.03e0

VQSLOD
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SIO_000300: -1.215e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

DP
type: SiteQuality
SIO_000300: 2.489424e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.887e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16504
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: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

African
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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: 8652
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.22e-1

BaseQRankSum
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SIO_000300: -4.535e0

DP
type: SiteQuality
SIO_000300: 2.489575e6

MQRankSum
type: SiteQuality
SIO_000300: -5.08e-1

FS
type: SiteQuality
SIO_000300: 8.595000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.991e1

QD
type: SiteQuality
SIO_000300: 1.342e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3537
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

East Asian
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: 3
allele frequency: 1.817961459217065e-4
allele num: 16502
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

ReadPosRankSum
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.931e1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.199e1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.52e-1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

African
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allele frequency: 6.732063858434314e-4
allele num: 10398
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.489691e6

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

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

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

African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
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 frequency: 0.0e0
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num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: 1.01e0

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

African
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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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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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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South Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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Latino
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QD
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ReadPosRankSum
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BaseQRankSum
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FS
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MQ
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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MQ
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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South Asian
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European (Non-Finnish)
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Other
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ClippingRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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VQSLOD
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ReadPosRankSum
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FS
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QD
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MQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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Other
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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QD
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VQSLOD
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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South Asian
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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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DP
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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QD
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MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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MQ
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QD
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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GenotypeQuality
all individuals: 2694
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.594706798131811e-4
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.651007114339747e-4
allele num: 66626
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.23e1

DP
type: SiteQuality
SIO_000300: 2.484392e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

MQRankSum
type: SiteQuality
SIO_000300: -6.286e0

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.062e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

GenotypeDepth
all individuals: 1621
bin: 6.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20947
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2687
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 2.25e1
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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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4555
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variant carriers: 0

GenotypeQuality
all individuals: 3539
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.88e-1

MQ
type: SiteQuality
SIO_000300: 5.817e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 1.0425e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.66e-1

QD
type: SiteQuality
SIO_000300: 1.15e1

DP
type: SiteQuality
SIO_000300: 2.477338e6

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.18e-1

GenotypeDepth
all individuals: 1068
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variant carriers: 1

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 115
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4550
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.090875867949811e-5
allele num: 16418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503714174009804e-5
allele num: 66502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

DP
type: SiteQuality
SIO_000300: 2.474662e6

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.723e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

FS
type: SiteQuality
SIO_000300: 9.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.416e1

GenotypeDepth
all individuals: 1094
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
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variant carriers: 0

GenotypeQuality
all individuals: 126
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variant carriers: 0

GenotypeQuality
all individuals: 551
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2054
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 15443
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 4094
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2680
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variant carriers: 0

GenotypeQuality
all individuals: 19
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20946
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4549
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50407604608489e-5
allele num: 66486
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.837e1

DP
type: SiteQuality
SIO_000300: 2.4727e6

VQSLOD
type: SiteQuality
SIO_000300: -2.576e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.632e0

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

GenotypeQuality
all individuals: 6320
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 4543
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 2678
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 143
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GenotypeQuality
all individuals: 173
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variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 646
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4093
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2054
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20945
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15334
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505117399157134e-5
allele num: 66440
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.79e-1

FS
type: SiteQuality
SIO_000300: 4.646e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.470313e6

QD
type: SiteQuality
SIO_000300: 1.086e1

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 143
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 2054
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 4093
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.763718023823472e-5
allele num: 10242
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

FS
type: SiteQuality
SIO_000300: 4.646e0

QD
type: SiteQuality
SIO_000300: 1.086e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.79e-1

DP
type: SiteQuality
SIO_000300: 2.470313e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15195
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.773260359655981e-5
allele num: 10232
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.475e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.126700159294204e-5
allele num: 16322
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.122e0

DP
type: SiteQuality
SIO_000300: 2.431788e6

VQSLOD
type: SiteQuality
SIO_000300: 8.41e-1

QD
type: SiteQuality
SIO_000300: 1.082e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.024620410138528e-5
allele num: 66124
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.879470460383324e-5
allele num: 10122
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.56e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

DP
type: SiteQuality
SIO_000300: 2.426561e6

VQSLOD
type: SiteQuality
SIO_000300: 9.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.75e-1

QD
type: SiteQuality
SIO_000300: 1.264e1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.188884762965714e-5
allele num: 16158
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.06e0

QD
type: SiteQuality
SIO_000300: 1.353e1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

DP
type: SiteQuality
SIO_000300: 2.353955e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.08e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4240
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 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
allele num: 10360
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21580547112462e-4
allele num: 16450
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e-1

FS
type: SiteQuality
SIO_000300: 5.774e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.963e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

DP
type: SiteQuality
SIO_000300: 2.508483e6

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

FS
type: SiteQuality
SIO_000300: 3.9e0

VQSLOD
type: SiteQuality
SIO_000300: -2.652e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: 2.94e0

QD
type: SiteQuality
SIO_000300: 9.24e0

DP
type: SiteQuality
SIO_000300: 2.508967e6

MQRankSum
type: SiteQuality
SIO_000300: -9.62e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.69e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 2
allele frequency: 1.93050193050193e-4
allele num: 10360
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 7.76e-1

DP
type: SiteQuality
SIO_000300: 2.509191e6

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50195253829979e-5
allele num: 66580
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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DP
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BaseQRankSum
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MQRankSum
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SIO_000300: 2.81e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 102
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variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

DP
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FS
type: SiteQuality
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: 2.0e-4

ClippingRankSum
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SIO_000300: 3.6e-1

MQ
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SIO_000300: 5.985e1

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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South Asian
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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FS
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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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ReadPosRankSum
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SIO_000300: 2.16e0

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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DP
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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MQ
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MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

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

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

VQSLOD
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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SIO_000300: 6.419e0

ReadPosRankSum
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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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: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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num of homozygotes: 0

MQRankSum
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SIO_000300: 8.139999999999999e-1

InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
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DP
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MQ
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SIO_000300: 6.0e1

VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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SIO_000300: 4.78e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

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

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

African
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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 num: 8636
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 4.78e0

ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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FS
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66622
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Latino
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num of homozygotes: 0

East Asian
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African
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Other
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MQRankSum
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DP
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

African
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Latino
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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QD
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VQSLOD
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MQ
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SIO_000300: 5.919e1

ClippingRankSum
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SIO_000300: -9.45e-1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele num: 66648
num of homozygotes: 0

African
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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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Other
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Latino
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FS
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MQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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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)
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allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

African
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South Asian
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Other
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Latino
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European (Finnish)
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East Asian
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QD
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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SIO_000300: -3.1e-2

MQ
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SIO_000300: 5.897e1

GenotypeDepth
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variant carriers: 1

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

African
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allele frequency: 0.0e0
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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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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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South 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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MQ
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MQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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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 frequency: 5.186721991701245e-4
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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African
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East Asian
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European (Finnish)
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FS
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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DP
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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
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GenotypeQuality
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African
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allele num: 10372
num of homozygotes: 0

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

Other
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European (Non-Finnish)
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African
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East Asian
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South Asian
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European (Finnish)
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InbreedingCoeff
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MQ
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VQSLOD
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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MQRankSum
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FS
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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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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Other
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VQSLOD
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DP
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QD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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African
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European (Finnish)
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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FS
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BaseQRankSum
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ReadPosRankSum
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MQ
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QD
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InbreedingCoeff
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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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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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ClippingRankSum
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VQSLOD
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QD
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQ
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BaseQRankSum
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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 num: 10372
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Other
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MQ
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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East Asian
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Other
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Latino
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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QD
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FS
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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FS
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ReadPosRankSum
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ClippingRankSum
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DP
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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FS
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MQRankSum
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QD
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VQSLOD
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DP
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MQ
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5229
bin: 8.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 9.151999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

DP
type: SiteQuality
SIO_000300: 2.514019e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.538e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.329e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.877e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-1

GenotypeQuality
all individuals: 220
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18319
bin: 9.75e1
variant carriers: 78

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 4247
bin: 9.25e1
variant carriers: 0

African
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allele count: 3
allele frequency: 2.893518518518518e-4
allele num: 10368
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.462004500605851e-4
allele num: 11554
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: 906
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 4.953170028818444e-4
allele num: 66624
num of homozygotes: 0

South Asian
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allele count: 38
allele frequency: 2.304147465437788e-3
allele num: 16492
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.78e-1

DP
type: SiteQuality
SIO_000300: 2.513859e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

QD
type: SiteQuality
SIO_000300: 1.491e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 169
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variant carriers: 0

GenotypeQuality
all individuals: 3566
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.632e0

QD
type: SiteQuality
SIO_000300: 1.526e1

FS
type: SiteQuality
SIO_000300: 3.069e0

VQSLOD
type: SiteQuality
SIO_000300: -6.169e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.506117e6

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.722e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

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: 8
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 56

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12103
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GenotypeQuality
all individuals: 7523
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 55
allele frequency: 3.334950278923114e-3
allele num: 16492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.501184e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.489e1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.77e0

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

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 86
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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: 8
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GenotypeQuality
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GenotypeQuality
all individuals: 7523
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3555
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variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
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variant carriers: 0

GenotypeQuality
all individuals: 4242
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 5769
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003093185981561e-5
allele num: 66598
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.489e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

DP
type: SiteQuality
SIO_000300: 2.501184e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
all individuals: 10
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
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: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

FS
type: SiteQuality
SIO_000300: 1.477e0

VQSLOD
type: SiteQuality
SIO_000300: 2.69e-1

DP
type: SiteQuality
SIO_000300: 2.487263e6

BaseQRankSum
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SIO_000300: 4.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQRankSum
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SIO_000300: 7.03e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.664e1

GenotypeQuality
all individuals: 131
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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: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 26
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.14e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.475829e6

QD
type: SiteQuality
SIO_000300: 2.115e1

BaseQRankSum
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SIO_000300: 6.18e0

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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variant carriers: 1

GenotypeQuality
all individuals: 617
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GenotypeQuality
all individuals: 2170
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.087604507451835e-5
allele num: 11004
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64378
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.409413e6

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 8.470000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.838e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

GenotypeQuality
all individuals: 143
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2764
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2739
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28264
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3059
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8179
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4626
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2793
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 3.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551109042965721e-5
allele num: 64470
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.15e-1

QD
type: SiteQuality
SIO_000300: 1.637e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.369999999999999e0

FS
type: SiteQuality
SIO_000300: 3.555e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 3.414004e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-1

GenotypeDepth
all individuals: 1119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3019
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28263
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 169
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3067
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4688
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2764
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8939
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2796
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12356
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541782300339192e-5
allele num: 64860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
SIO_000300: -9.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.865e-1

DP
type: SiteQuality
SIO_000300: 3.430291e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.399e0

QD
type: SiteQuality
SIO_000300: 1.379e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.02e-1

FS
type: SiteQuality
SIO_000300: 5.337e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 11841
bin: 6.25e1
variant carriers: 0