2-169948428-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948428
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948428
    reference: chr 2
allele count: 2
allele frequency: 1.660605456749531e-5
allele num: 120438
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.701T>C
  hgvsp: ENSP00000407747.1:p.Ile234Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.701T>C
  hgvsp: ENSP00000316670.4:p.Ile234Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.701T>C
  hgvsp: ENSP00000407167.2:p.Ile234Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.701T>C
  hgvsp: ENSP00000473337.1:p.Ile234Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.260T>C
  hgvsp: ENSP00000388066.1:p.Ile87Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.881T>C
  hgvsp: ENSP00000389241.2:p.Ile294Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.701T>C
  hgvsp: ENSP00000388564.1:p.Ile234Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.701T>C
  hgvsp: ENSP00000350154.2:p.Ile234Thr
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8347
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3062
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile234Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-169948438-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948438
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948438
    reference: chr 2
allele count: 1
allele frequency: 8.328336331534413e-6
allele num: 120072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.711A>C
  hgvsp: ENSP00000407167.2:p.Gln237His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.711A>C
  hgvsp: ENSP00000388564.1:p.Gln237His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.711A>C
  hgvsp: ENSP00000473337.1:p.Gln237His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.711A>C
  hgvsp: ENSP00000350154.2:p.Gln237His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.711A>C
  hgvsp: ENSP00000407747.1:p.Gln237His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.270A>C
  hgvsp: ENSP00000388066.1:p.Gln90His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.891A>C
  hgvsp: ENSP00000389241.2:p.Gln297His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.711A>C
  hgvsp: ENSP00000316670.4:p.Gln237His
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41771
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln237His
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

2-169948439-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948439
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948439
    reference: chr 2
allele count: 13
allele frequency: 1.083369445648188e-4
allele num: 119996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.712T>C
  hgvsp: ENSP00000407747.1:p.Tyr238His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.712T>C
  hgvsp: ENSP00000473337.1:p.Tyr238His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.271T>C
  hgvsp: ENSP00000388066.1:p.Tyr91His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.892T>C
  hgvsp: ENSP00000389241.2:p.Tyr298His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.712T>C
  hgvsp: ENSP00000316670.4:p.Tyr238His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.712T>C
  hgvsp: ENSP00000350154.2:p.Tyr238His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.712T>C
  hgvsp: ENSP00000407167.2:p.Tyr238His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.712T>C
  hgvsp: ENSP00000388564.1:p.Tyr238His
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27022
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41651
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr238His
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-169948441-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948441
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948441
    reference: chr 2
allele count: 4
allele frequency: 3.33889816360601e-5
allele num: 119800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.273T>C
  hgvsp: ENST00000421653.1:c.273T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.714T>C
  hgvsp: ENST00000436483.2:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.714T>C
  hgvsp: ENST00000327239.4:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.714T>C
  hgvsp: ENST00000357546.2:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.714T>C
  hgvsp: ENST00000428522.1:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.894T>C
  hgvsp: ENST00000432060.2:c.894T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.714T>C
  hgvsp: ENST00000412271.1:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.714T>C
  hgvsp: ENST00000602501.1:c.714T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7847
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr238Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

2-169948455-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948455
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948455
    reference: chr 2
allele count: 2
allele frequency: 1.686198465559396e-5
allele num: 118610
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.728T>C
  hgvsp: ENSP00000316670.4:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.728T>C
  hgvsp: ENSP00000350154.2:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.728T>C
  hgvsp: ENSP00000473337.1:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.728T>C
  hgvsp: ENSP00000407747.1:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.728T>C
  hgvsp: ENSP00000407167.2:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.287T>C
  hgvsp: ENSP00000388066.1:p.Ile96Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.908T>C
  hgvsp: ENSP00000389241.2:p.Ile303Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.728T>C
  hgvsp: ENSP00000388564.1:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17423
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2514
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile243Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS

2-169948465-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948465
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948465
    reference: chr 2
allele count: 1
allele frequency: 8.558126797206627e-6
allele num: 116848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+2T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+2T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+2T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+2T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+2T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+2T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+2T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+2T>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3042
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36085
  bin: 6.25e1
  variant carriers: 0
hgvs: c.736+2T>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

2-169948468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948468
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948468
    reference: chr 2
allele count: 1
allele frequency: 8.634236474468563e-6
allele num: 115818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+5G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+5G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+5G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+5G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+5G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+5G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+5G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+5G>A
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7236
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32411
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
hgvs: c.736+5G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

2-169948471-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948471
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948471
    reference: chr 2
allele count: 1
allele frequency: 8.650968043324048e-6
allele num: 115594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+8T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+8T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+8T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+8T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+8T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+8T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+8T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+8T>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6454
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 3.25e1
  variant carriers: 0
hgvs: c.736+8T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

2-169948473-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948473
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948473
    reference: chr 2
allele count: 2
allele frequency: 1.738979219198331e-5
allele num: 115010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+10C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+10C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+10C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+10C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+10C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+10C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+10C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+10C>T
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3040
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6095
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

2-169948474-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948474
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948474
    reference: chr 2
allele count: 1
allele frequency: 8.696559641006019e-6
allele num: 114988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+11G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+11G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+11G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+11G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+11G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+11G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+11G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+11G>A
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21638
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2060
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3038
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-169948474-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948474
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948474
    reference: chr 2
allele count: 1
allele frequency: 8.696559641006019e-6
allele num: 114988
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+11G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+11G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+11G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+11G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+11G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+11G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+11G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+11G>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2574
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

2-169948477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948477
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948477
    reference: chr 2
allele count: 7
allele frequency: 6.124663143527106e-5
allele num: 114292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+14C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+14C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+14C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+14C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+14C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+14C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+14C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+14C>T
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9072
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13875
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7353
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3035
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

2-169948478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948478
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948478
    reference: chr 2
allele count: 9
allele frequency: 7.885191610156126e-5
allele num: 114138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+15G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+15G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+15G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+15G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+15G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+15G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+15G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+15G>A
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13777
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9424
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19953
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28643
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

2-169948480-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948480
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948479
    reference: chr 2
allele count: 1
allele frequency: 8.764549151591641e-6
allele num: 114096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+18delG
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+18delG
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+18delG
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+18delG
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+18delG
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+18delG
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+18delG
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+18delG
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10096
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2689
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3595
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: TG
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

2-169948486-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948486
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948486
    reference: chr 2
allele count: 3
allele frequency: 2.648772735299311e-5
allele num: 113260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+23T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+23T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+23T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+23T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+23T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+23T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+23T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+23T>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17030
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24676
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3353
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum

2-169948488-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948488
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948488
    reference: chr 2
allele count: 1
allele frequency: 8.841889334913084e-6
allele num: 113098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+25T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+25T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+25T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+25T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+25T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+25T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+25T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+25T>A
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11349
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9161
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22672
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

2-169948504-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948504
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948504
    reference: chr 2
allele count: 1
allele frequency: 9.023967658099914e-6
allele num: 110816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+41G>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+41G>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+41G>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+41G>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+41G>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+41G>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+41G>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+41G>T
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7578
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3000
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11604
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3635
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4534
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

2-169948511-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948511
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948511
    reference: chr 2
allele count: 8
allele frequency: 7.321314175894573e-5
allele num: 109270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+48A>G
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+48A>G
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+48A>G
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+48A>G
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+48A>G
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+48A>G
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+48A>G
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+48A>G
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13378
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15988
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11196
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6943
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8626
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4558
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5415
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2582
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

2-169948514-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169948514
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169948514
    reference: chr 2
allele count: 2
allele frequency: 1.86894927671663e-5
allele num: 107012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.736+51G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.736+51G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.916+51G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.736+51G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.295+51G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.736+51G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.736+51G>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.736+51G>A
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15880
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3592
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2702
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7775
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

2-169952003-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952003
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952003
    reference: chr 2
allele count: 23
allele frequency: 1.920507682030728e-4
allele num: 119760
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-51C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-51C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-51C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-51C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-51C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-51C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-51C>T
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-51C>T
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5236
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18433
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

2-169952004-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952004
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952004
    reference: chr 2
allele count: 16
allele frequency: 1.334979808430397e-4
allele num: 119852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-50T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-50T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-50T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-50T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-50T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-50T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-50T>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-50T>A
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23307
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22980
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/2-169952008-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952008
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952008
    reference: chr 2
allele count: 1
allele frequency: 8.346688034188035e-6
allele num: 119808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-46C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-46C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-46C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-46C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-46C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-46C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-46C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-46C>A
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

2-169952019-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952019
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952019
    reference: chr 2
allele count: 1
allele frequency: 8.335000333400014e-6
allele num: 119976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-35T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-35T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-35T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-35T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-35T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-35T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-35T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-35T>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7743
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

http://identifiers.org/exac.variant/2-169952022-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952022
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952022
    reference: chr 2
allele count: 2
allele frequency: 1.666444474070124e-5
allele num: 120016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-32C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-32C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-32C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-32C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-32C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-32C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-32C>A
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-32C>A
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5235
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25106
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

2-169952028-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952028
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952028
    reference: chr 2
allele count: 7
allele frequency: 5.823724188422437e-5
allele num: 120198
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-26G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-26G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-26G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-26G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-26G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-26G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-26G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-26G>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/2-169952030-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952030
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952030
    reference: chr 2
allele count: 1
allele frequency: 8.315316813570598e-6
allele num: 120260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-24A>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-24A>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-24A>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-24A>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-24A>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-24A>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-24A>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-24A>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

2-169952035-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952035
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952035
    reference: chr 2
allele count: 2
allele frequency: 1.660908849322349e-5
allele num: 120416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-19T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-19T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-19T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-19T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-19T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-19T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-19T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-19T>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5362
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

2-169952037-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952037
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952038
    reference: chr 2
allele count: 8
allele frequency: 6.640877924061562e-5
allele num: 120466
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-13dupT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-13dupT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-13dupT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-13dupT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-13dupT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-13dupT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-13dupT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-13dupT
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26006
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5370
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

2-169952043-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952043
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952043
    reference: chr 2
allele count: 1
allele frequency: 8.290361625574107e-6
allele num: 120622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-11T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-11T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-11T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-11T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-11T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-11T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-11T>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-11T>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

2-169952043-T-TCTAGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952043
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952048
    reference: chr 2
allele count: 8
allele frequency: 6.632289300459286e-5
allele num: 120622
alternate allele: TCTAGA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-9_737-8insAGACT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-9_737-8insAGACT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-9_737-8insAGACT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-9_917-8insAGACT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-9_737-8insAGACT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-9_737-8insAGACT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-9_737-8insAGACT
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-9_296-8insAGACT
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

2-169952053-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952053
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952053
    reference: chr 2
allele count: 123
allele frequency: 1.0172351053624e-3
allele num: 120916
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737-1G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737-1G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737-1G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737-1G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737-1G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917-1G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296-1G>C
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737-1G>C
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7555
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 9.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19344
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 7.75e1
  variant carriers: 0
hgvs: c.737-1G>C
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

2-169952054-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952054
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952054
    reference: chr 2
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.737G>T
  hgvsp: ENSP00000350154.2:p.Ser246Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.917G>T
  hgvsp: ENSP00000389241.2:p.Ser306Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.737G>T
  hgvsp: ENSP00000473337.1:p.Ser246Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.737G>T
  hgvsp: ENSP00000316670.4:p.Ser246Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.296G>T
  hgvsp: ENSP00000388066.1:p.Ser99Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.737G>T
  hgvsp: ENSP00000407747.1:p.Ser246Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.737G>T
  hgvsp: ENSP00000388564.1:p.Ser246Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.737G>T
  hgvsp: ENSP00000407167.2:p.Ser246Ile
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser246Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/2-169952062-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952062
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952062
    reference: chr 2
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.925A>C
  hgvsp: ENSP00000389241.2:p.Lys309Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.745A>C
  hgvsp: ENSP00000316670.4:p.Lys249Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.745A>C
  hgvsp: ENSP00000388564.1:p.Lys249Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.745A>C
  hgvsp: ENSP00000473337.1:p.Lys249Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.745A>C
  hgvsp: ENSP00000350154.2:p.Lys249Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.745A>C
  hgvsp: ENSP00000407747.1:p.Lys249Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.304A>C
  hgvsp: ENSP00000388066.1:p.Lys102Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.745A>C
  hgvsp: ENSP00000407167.2:p.Lys249Gln
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys249Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-169952068-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952068
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952068
    reference: chr 2
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.751A>C
  hgvsp: ENSP00000316670.4:p.Lys251Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.751A>C
  hgvsp: ENSP00000350154.2:p.Lys251Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.310A>C
  hgvsp: ENSP00000388066.1:p.Lys104Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.751A>C
  hgvsp: ENSP00000407747.1:p.Lys251Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.751A>C
  hgvsp: ENSP00000388564.1:p.Lys251Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.751A>C
  hgvsp: ENSP00000407167.2:p.Lys251Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.751A>C
  hgvsp: ENSP00000473337.1:p.Lys251Gln
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.931A>C
  hgvsp: ENSP00000389241.2:p.Lys311Gln
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys251Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-169952068-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952068
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952068
    reference: chr 2
allele count: 5
allele frequency: 4.125072188763303e-5
allele num: 121210
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.751A>G
  hgvsp: ENSP00000316670.4:p.Lys251Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.751A>G
  hgvsp: ENSP00000407747.1:p.Lys251Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.931A>G
  hgvsp: ENSP00000389241.2:p.Lys311Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.751A>G
  hgvsp: ENSP00000388564.1:p.Lys251Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.751A>G
  hgvsp: ENSP00000350154.2:p.Lys251Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.751A>G
  hgvsp: ENSP00000473337.1:p.Lys251Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.310A>G
  hgvsp: ENSP00000388066.1:p.Lys104Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.751A>G
  hgvsp: ENSP00000407167.2:p.Lys251Glu
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys251Glu
num of homozygotes: 1
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-169952081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952081
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952081
    reference: chr 2
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.764C>T
  hgvsp: ENSP00000407167.2:p.Ser255Phe
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.944C>T
  hgvsp: ENSP00000389241.2:p.Ser315Phe
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.764C>T
  hgvsp: ENSP00000407747.1:p.Ser255Phe
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.764C>T
  hgvsp: ENSP00000473337.1:p.Ser255Phe
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.764C>T
  hgvsp: ENSP00000388564.1:p.Ser255Phe
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.764C>T
  hgvsp: ENSP00000316670.4:p.Ser255Phe
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.764C>T
  hgvsp: ENSP00000350154.2:p.Ser255Phe
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.323C>T
  hgvsp: ENSP00000388066.1:p.Ser108Phe
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26800
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22935
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser255Phe
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ

2-169952084-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952084
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952084
    reference: chr 2
allele count: 128
allele frequency: 1.055147968015827e-3
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.947A>G
  hgvsp: ENSP00000389241.2:p.Tyr316Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.767A>G
  hgvsp: ENSP00000473337.1:p.Tyr256Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.326A>G
  hgvsp: ENSP00000388066.1:p.Tyr109Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.767A>G
  hgvsp: ENSP00000407747.1:p.Tyr256Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.767A>G
  hgvsp: ENSP00000316670.4:p.Tyr256Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.767A>G
  hgvsp: ENSP00000350154.2:p.Tyr256Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.767A>G
  hgvsp: ENSP00000407167.2:p.Tyr256Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.767A>G
  hgvsp: ENSP00000388564.1:p.Tyr256Cys
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 9.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7592
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22969
  bin: 9.75e1
  variant carriers: 127
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr256Cys
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

2-169952086-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952086
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952086
    reference: chr 2
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.949G>T
  hgvsp: ENSP00000389241.2:p.Val317Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.769G>T
  hgvsp: ENSP00000407167.2:p.Val257Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.328G>T
  hgvsp: ENSP00000388066.1:p.Val110Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.769G>T
  hgvsp: ENSP00000473337.1:p.Val257Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.769G>T
  hgvsp: ENSP00000388564.1:p.Val257Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.769G>T
  hgvsp: ENSP00000407747.1:p.Val257Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.769G>T
  hgvsp: ENSP00000316670.4:p.Val257Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.769G>T
  hgvsp: ENSP00000350154.2:p.Val257Leu
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26835
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val257Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

2-169952105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952105
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952105
    reference: chr 2
allele count: 2
allele frequency: 1.648396933981703e-5
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.788C>T
  hgvsp: ENSP00000407747.1:p.Pro263Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.788C>T
  hgvsp: ENSP00000388564.1:p.Pro263Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.788C>T
  hgvsp: ENSP00000473337.1:p.Pro263Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.788C>T
  hgvsp: ENSP00000316670.4:p.Pro263Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.968C>T
  hgvsp: ENSP00000389241.2:p.Pro323Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.347C>T
  hgvsp: ENSP00000388066.1:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.788C>T
  hgvsp: ENSP00000350154.2:p.Pro263Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.788C>T
  hgvsp: ENSP00000407167.2:p.Pro263Leu
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22898
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro263Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

2-169952106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952106
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952106
    reference: chr 2
allele count: 10
allele frequency: 8.241712957621112e-5
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.348G>A
  hgvsp: ENST00000421653.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.789G>A
  hgvsp: ENST00000412271.1:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.789G>A
  hgvsp: ENST00000428522.1:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.789G>A
  hgvsp: ENST00000436483.2:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.969G>A
  hgvsp: ENST00000432060.2:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.789G>A
  hgvsp: ENST00000602501.1:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.789G>A
  hgvsp: ENST00000327239.4:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.789G>A
  hgvsp: ENST00000357546.2:c.789G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5489
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22899
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro263Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

2-169952106-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952106
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952106
    reference: chr 2
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.789G>T
  hgvsp: ENST00000436483.2:c.789G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.789G>T
  hgvsp: ENST00000412271.1:c.789G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.789G>T
  hgvsp: ENST00000428522.1:c.789G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.789G>T
  hgvsp: ENST00000327239.4:c.789G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.789G>T
  hgvsp: ENST00000357546.2:c.789G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.969G>T
  hgvsp: ENST00000432060.2:c.969G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.348G>T
  hgvsp: ENST00000421653.1:c.348G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.789G>T
  hgvsp: ENST00000602501.1:c.789G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro263Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

2-169952108-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952108
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952108
    reference: chr 2
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.791T>C
  hgvsp: ENSP00000388564.1:p.Val264Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.971T>C
  hgvsp: ENSP00000389241.2:p.Val324Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.791T>C
  hgvsp: ENSP00000473337.1:p.Val264Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.791T>C
  hgvsp: ENSP00000407747.1:p.Val264Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.791T>C
  hgvsp: ENSP00000316670.4:p.Val264Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.350T>C
  hgvsp: ENSP00000388066.1:p.Val117Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.791T>C
  hgvsp: ENSP00000407167.2:p.Val264Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.791T>C
  hgvsp: ENSP00000350154.2:p.Val264Ala
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val264Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

2-169952110-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952110
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952110
    reference: chr 2
allele count: 3
allele frequency: 2.472513887286333e-5
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.793G>C
  hgvsp: ENSP00000388564.1:p.Val265Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.793G>C
  hgvsp: ENSP00000407747.1:p.Val265Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.793G>C
  hgvsp: ENSP00000350154.2:p.Val265Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.793G>C
  hgvsp: ENSP00000473337.1:p.Val265Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.793G>C
  hgvsp: ENSP00000407167.2:p.Val265Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.793G>C
  hgvsp: ENSP00000316670.4:p.Val265Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.973G>C
  hgvsp: ENSP00000389241.2:p.Val325Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.352G>C
  hgvsp: ENSP00000388066.1:p.Val118Leu
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val265Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

2-169952112-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952112
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952112
    reference: chr 2
allele count: 14
allele frequency: 1.153858833613556e-4
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.795A>G
  hgvsp: ENST00000428522.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.354A>G
  hgvsp: ENST00000421653.1:c.354A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.795A>G
  hgvsp: ENST00000357546.2:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.795A>G
  hgvsp: ENST00000327239.4:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.975A>G
  hgvsp: ENST00000432060.2:c.975A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.795A>G
  hgvsp: ENST00000436483.2:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.795A>G
  hgvsp: ENST00000412271.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.795A>G
  hgvsp: ENST00000602501.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26850
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val265Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff

2-169952114-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952114
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952114
    reference: chr 2
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.797A>G
  hgvsp: ENSP00000407747.1:p.Glu266Gly
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.977A>G
  hgvsp: ENSP00000389241.2:p.Glu326Gly
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.797A>G
  hgvsp: ENSP00000388564.1:p.Glu266Gly
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.797A>G
  hgvsp: ENSP00000350154.2:p.Glu266Gly
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.797A>G
  hgvsp: ENSP00000473337.1:p.Glu266Gly
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.797A>G
  hgvsp: ENSP00000407167.2:p.Glu266Gly
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.356A>G
  hgvsp: ENSP00000388066.1:p.Glu119Gly
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.797A>G
  hgvsp: ENSP00000316670.4:p.Glu266Gly
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu266Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

2-169952119-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952119
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952119
    reference: chr 2
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.982A>G
  hgvsp: ENSP00000389241.2:p.Met328Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.802A>G
  hgvsp: ENSP00000407167.2:p.Met268Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.361A>G
  hgvsp: ENSP00000388066.1:p.Met121Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.802A>G
  hgvsp: ENSP00000407747.1:p.Met268Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.802A>G
  hgvsp: ENSP00000350154.2:p.Met268Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.802A>G
  hgvsp: ENSP00000316670.4:p.Met268Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.802A>G
  hgvsp: ENSP00000388564.1:p.Met268Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.802A>G
  hgvsp: ENSP00000473337.1:p.Met268Val
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met268Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/2-169952124-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952124
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952124
    reference: chr 2
allele count: 6
allele frequency: 4.945190801945108e-5
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.987C>A
  hgvsp: ENSP00000389241.2:p.Asp329Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.366C>A
  hgvsp: ENSP00000388066.1:p.Asp122Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.807C>A
  hgvsp: ENSP00000407747.1:p.Asp269Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.807C>A
  hgvsp: ENSP00000316670.4:p.Asp269Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.807C>A
  hgvsp: ENSP00000388564.1:p.Asp269Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.807C>A
  hgvsp: ENSP00000407167.2:p.Asp269Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.807C>A
  hgvsp: ENSP00000473337.1:p.Asp269Glu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.807C>A
  hgvsp: ENSP00000350154.2:p.Asp269Glu
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp269Glu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

2-169952127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952127
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952127
    reference: chr 2
allele count: 7
allele frequency: 5.769199070334778e-5
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.990C>T
  hgvsp: ENST00000432060.2:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.810C>T
  hgvsp: ENST00000412271.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.369C>T
  hgvsp: ENST00000421653.1:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.810C>T
  hgvsp: ENST00000327239.4:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.810C>T
  hgvsp: ENST00000436483.2:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.810C>T
  hgvsp: ENST00000602501.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.810C>T
  hgvsp: ENST00000357546.2:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.810C>T
  hgvsp: ENST00000428522.1:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26846
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5489
  bin: 6.75e1
  variant carriers: 0
hgvs: p.His270His
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-169952135-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952135
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952135
    reference: chr 2
allele count: 2
allele frequency: 1.648451280022419e-5
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.818C>G
  hgvsp: ENSP00000388564.1:p.Thr273Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.818C>G
  hgvsp: ENSP00000407167.2:p.Thr273Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.818C>G
  hgvsp: ENSP00000350154.2:p.Thr273Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.377C>G
  hgvsp: ENSP00000388066.1:p.Thr126Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.818C>G
  hgvsp: ENSP00000473337.1:p.Thr273Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.818C>G
  hgvsp: ENSP00000407747.1:p.Thr273Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.818C>G
  hgvsp: ENSP00000316670.4:p.Thr273Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.998C>G
  hgvsp: ENSP00000389241.2:p.Thr333Arg
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr273Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

2-169952138-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952138
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952138
    reference: chr 2
allele count: 9
allele frequency: 7.418030760100886e-5
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.821G>A
  hgvsp: ENSP00000388564.1:p.Ser274Asn
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.821G>A
  hgvsp: ENSP00000407747.1:p.Ser274Asn
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.821G>A
  hgvsp: ENSP00000316670.4:p.Ser274Asn
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.380G>A
  hgvsp: ENSP00000388066.1:p.Ser127Asn
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1001G>A
  hgvsp: ENSP00000389241.2:p.Ser334Asn
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.821G>A
  hgvsp: ENSP00000407167.2:p.Ser274Asn
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.821G>A
  hgvsp: ENSP00000350154.2:p.Ser274Asn
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.821G>A
  hgvsp: ENSP00000473337.1:p.Ser274Asn
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22895
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser274Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-169952138-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952138
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952138
    reference: chr 2
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.821G>T
  hgvsp: ENSP00000316670.4:p.Ser274Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.821G>T
  hgvsp: ENSP00000350154.2:p.Ser274Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.821G>T
  hgvsp: ENSP00000407747.1:p.Ser274Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.380G>T
  hgvsp: ENSP00000388066.1:p.Ser127Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.821G>T
  hgvsp: ENSP00000388564.1:p.Ser274Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1001G>T
  hgvsp: ENSP00000389241.2:p.Ser334Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.821G>T
  hgvsp: ENSP00000407167.2:p.Ser274Ile
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.821G>T
  hgvsp: ENSP00000473337.1:p.Ser274Ile
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22895
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser274Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

2-169952143-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952143
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952143
    reference: chr 2
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.826T>C
  hgvsp: ENSP00000316670.4:p.Phe276Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.826T>C
  hgvsp: ENSP00000473337.1:p.Phe276Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1006T>C
  hgvsp: ENSP00000389241.2:p.Phe336Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.826T>C
  hgvsp: ENSP00000350154.2:p.Phe276Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.826T>C
  hgvsp: ENSP00000407167.2:p.Phe276Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.826T>C
  hgvsp: ENSP00000407747.1:p.Phe276Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.826T>C
  hgvsp: ENSP00000388564.1:p.Phe276Leu
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.385T>C
  hgvsp: ENSP00000388066.1:p.Phe129Leu
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe276Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-169952151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952151
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952151
    reference: chr 2
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.834G>A
  hgvsp: ENST00000602501.1:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1014G>A
  hgvsp: ENST00000432060.2:c.1014G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.393G>A
  hgvsp: ENST00000421653.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.834G>A
  hgvsp: ENST00000436483.2:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.834G>A
  hgvsp: ENST00000412271.1:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.834G>A
  hgvsp: ENST00000327239.4:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.834G>A
  hgvsp: ENST00000428522.1:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.834G>A
  hgvsp: ENST00000357546.2:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1758
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys278Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

2-169952155-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952155
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952155
    reference: chr 2
allele count: 8
allele frequency: 6.594022518586901e-5
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.838C>T
  hgvsp: ENSP00000407167.2:p.His280Tyr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.838C>T
  hgvsp: ENSP00000316670.4:p.His280Tyr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1018C>T
  hgvsp: ENSP00000389241.2:p.His340Tyr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.838C>T
  hgvsp: ENSP00000407747.1:p.His280Tyr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.838C>T
  hgvsp: ENSP00000388564.1:p.His280Tyr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.838C>T
  hgvsp: ENSP00000473337.1:p.His280Tyr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.397C>T
  hgvsp: ENSP00000388066.1:p.His133Tyr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.838C>T
  hgvsp: ENSP00000350154.2:p.His280Tyr
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5201
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22887
  bin: 9.75e1
  variant carriers: 8
hgvs: p.His280Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-169952159-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952159
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952159
    reference: chr 2
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.842A>G
  hgvsp: ENSP00000316670.4:p.Tyr281Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.842A>G
  hgvsp: ENSP00000388564.1:p.Tyr281Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.842A>G
  hgvsp: ENSP00000407167.2:p.Tyr281Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.842A>G
  hgvsp: ENSP00000350154.2:p.Tyr281Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.401A>G
  hgvsp: ENSP00000388066.1:p.Tyr134Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.842A>G
  hgvsp: ENSP00000407747.1:p.Tyr281Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1022A>G
  hgvsp: ENSP00000389241.2:p.Tyr341Cys
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.842A>G
  hgvsp: ENSP00000473337.1:p.Tyr281Cys
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26834
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1545
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr281Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-169952163-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952163
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952163
    reference: chr 2
allele count: 12
allele frequency: 9.891686037885158e-5
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.846C>T
  hgvsp: ENST00000357546.2:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.846C>T
  hgvsp: ENST00000436483.2:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.846C>T
  hgvsp: ENST00000327239.4:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1026C>T
  hgvsp: ENST00000432060.2:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.846C>T
  hgvsp: ENST00000412271.1:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.846C>T
  hgvsp: ENST00000602501.1:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.846C>T
  hgvsp: ENST00000428522.1:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.405C>T
  hgvsp: ENST00000421653.1:c.405C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala282Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

2-169952164-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952164
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952164
    reference: chr 2
allele count: 11
allele frequency: 9.067378868061394e-5
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.847G>A
  hgvsp: ENSP00000407167.2:p.Ala283Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.406G>A
  hgvsp: ENSP00000388066.1:p.Ala136Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.847G>A
  hgvsp: ENSP00000316670.4:p.Ala283Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.847G>A
  hgvsp: ENSP00000407747.1:p.Ala283Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1027G>A
  hgvsp: ENSP00000389241.2:p.Ala343Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.847G>A
  hgvsp: ENSP00000473337.1:p.Ala283Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.847G>A
  hgvsp: ENSP00000388564.1:p.Ala283Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.847G>A
  hgvsp: ENSP00000350154.2:p.Ala283Thr
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5198
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19557
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26825
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala283Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

2-169952166-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952166
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952166
    reference: chr 2
allele count: 2331
allele frequency: 1.921364985163205e-2
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.849T>C
  hgvsp: ENST00000412271.1:c.849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1029T>C
  hgvsp: ENST00000432060.2:c.1029T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.849T>C
  hgvsp: ENST00000357546.2:c.849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.849T>C
  hgvsp: ENST00000436483.2:c.849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.408T>C
  hgvsp: ENST00000421653.1:c.408T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.849T>C
  hgvsp: ENST00000327239.4:c.849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.849T>C
  hgvsp: ENST00000428522.1:c.849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.849T>C
  hgvsp: ENST00000602501.1:c.849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 9.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8912
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6684
  bin: 9.75e1
  variant carriers: 1984
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19452
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 8.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 6.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26668
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1710
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1511
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala283Ala
num of homozygotes: 97
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

2-169952167-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952167
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952167
    reference: chr 2
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.850G>A
  hgvsp: ENSP00000350154.2:p.Gly284Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1030G>A
  hgvsp: ENSP00000389241.2:p.Gly344Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.850G>A
  hgvsp: ENSP00000407747.1:p.Gly284Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.850G>A
  hgvsp: ENSP00000407167.2:p.Gly284Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.850G>A
  hgvsp: ENSP00000388564.1:p.Gly284Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.850G>A
  hgvsp: ENSP00000473337.1:p.Gly284Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.409G>A
  hgvsp: ENSP00000388066.1:p.Gly137Arg
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.850G>A
  hgvsp: ENSP00000316670.4:p.Gly284Arg
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27846
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly284Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-169952173-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952173
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952173
    reference: chr 2
allele count: 462
allele frequency: 3.808173560394995e-3
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.856G>C
  hgvsp: ENSP00000316670.4:p.Asp286His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.415G>C
  hgvsp: ENSP00000388066.1:p.Asp139His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1036G>C
  hgvsp: ENSP00000389241.2:p.Asp346His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.856G>C
  hgvsp: ENSP00000407747.1:p.Asp286His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.856G>C
  hgvsp: ENSP00000407167.2:p.Asp286His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.856G>C
  hgvsp: ENSP00000473337.1:p.Asp286His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.856G>C
  hgvsp: ENSP00000350154.2:p.Asp286His
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.856G>C
  hgvsp: ENSP00000388564.1:p.Asp286His
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 9.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 9.75e1
  variant carriers: 395
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27818
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp286His
num of homozygotes: 1
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

2-169952174-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952174
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952174
    reference: chr 2
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.857A>T
  hgvsp: ENSP00000388564.1:p.Asp286Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.416A>T
  hgvsp: ENSP00000388066.1:p.Asp139Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.857A>T
  hgvsp: ENSP00000350154.2:p.Asp286Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1037A>T
  hgvsp: ENSP00000389241.2:p.Asp346Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.857A>T
  hgvsp: ENSP00000407167.2:p.Asp286Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.857A>T
  hgvsp: ENSP00000407747.1:p.Asp286Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.857A>T
  hgvsp: ENSP00000473337.1:p.Asp286Val
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.857A>T
  hgvsp: ENSP00000316670.4:p.Asp286Val
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5720
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp286Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-169952194-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952194
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952194
    reference: chr 2
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.436C>G
  hgvsp: ENSP00000388066.1:p.Pro146Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.877C>G
  hgvsp: ENSP00000350154.2:p.Pro293Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.877C>G
  hgvsp: ENSP00000407167.2:p.Pro293Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.877C>G
  hgvsp: ENSP00000388564.1:p.Pro293Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.877C>G
  hgvsp: ENSP00000407747.1:p.Pro293Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1057C>G
  hgvsp: ENSP00000389241.2:p.Pro353Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.877C>G
  hgvsp: ENSP00000316670.4:p.Pro293Ala
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.877C>G
  hgvsp: ENSP00000473337.1:p.Pro293Ala
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro293Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

2-169952194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952194
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952194
    reference: chr 2
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1057C>T
  hgvsp: ENSP00000389241.2:p.Pro353Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.877C>T
  hgvsp: ENSP00000350154.2:p.Pro293Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.877C>T
  hgvsp: ENSP00000407747.1:p.Pro293Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.877C>T
  hgvsp: ENSP00000388564.1:p.Pro293Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.877C>T
  hgvsp: ENSP00000473337.1:p.Pro293Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.877C>T
  hgvsp: ENSP00000316670.4:p.Pro293Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.877C>T
  hgvsp: ENSP00000407167.2:p.Pro293Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.436C>T
  hgvsp: ENSP00000388066.1:p.Pro146Ser
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro293Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

2-169952199-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952199
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952199
    reference: chr 2
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1062G>C
  hgvsp: ENST00000432060.2:c.1062G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.882G>C
  hgvsp: ENST00000436483.2:c.882G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.441G>C
  hgvsp: ENST00000421653.1:c.441G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.882G>C
  hgvsp: ENST00000428522.1:c.882G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.882G>C
  hgvsp: ENST00000327239.4:c.882G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.882G>C
  hgvsp: ENST00000412271.1:c.882G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.882G>C
  hgvsp: ENST00000357546.2:c.882G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.882G>C
  hgvsp: ENST00000602501.1:c.882G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu294Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

2-169952207-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952207
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952207
    reference: chr 2
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.890T>C
  hgvsp: ENSP00000473337.1:p.Met297Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.890T>C
  hgvsp: ENSP00000350154.2:p.Met297Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.449T>C
  hgvsp: ENSP00000388066.1:p.Met150Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.890T>C
  hgvsp: ENSP00000316670.4:p.Met297Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.890T>C
  hgvsp: ENSP00000388564.1:p.Met297Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.890T>C
  hgvsp: ENSP00000407747.1:p.Met297Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.890T>C
  hgvsp: ENSP00000407167.2:p.Met297Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1070T>C
  hgvsp: ENSP00000389241.2:p.Met357Thr
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Met297Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-169952209-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952209
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952209
    reference: chr 2
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.892C>A
  hgvsp: ENSP00000473337.1:p.Pro298Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.451C>A
  hgvsp: ENSP00000388066.1:p.Pro151Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.892C>A
  hgvsp: ENSP00000407167.2:p.Pro298Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.892C>A
  hgvsp: ENSP00000388564.1:p.Pro298Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.892C>A
  hgvsp: ENSP00000407747.1:p.Pro298Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.892C>A
  hgvsp: ENSP00000316670.4:p.Pro298Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.892C>A
  hgvsp: ENSP00000350154.2:p.Pro298Thr
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1072C>A
  hgvsp: ENSP00000389241.2:p.Pro358Thr
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro298Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-169952209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952209
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952209
    reference: chr 2
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.892C>T
  hgvsp: ENSP00000473337.1:p.Pro298Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.892C>T
  hgvsp: ENSP00000316670.4:p.Pro298Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.892C>T
  hgvsp: ENSP00000350154.2:p.Pro298Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.892C>T
  hgvsp: ENSP00000407167.2:p.Pro298Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1072C>T
  hgvsp: ENSP00000389241.2:p.Pro358Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.892C>T
  hgvsp: ENSP00000407747.1:p.Pro298Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.892C>T
  hgvsp: ENSP00000388564.1:p.Pro298Ser
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.451C>T
  hgvsp: ENSP00000388066.1:p.Pro151Ser
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro298Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-169952219-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952219
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952219
    reference: chr 2
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.461T>A
  hgvsp: ENSP00000388066.1:p.Leu154Ter
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1082T>A
  hgvsp: ENSP00000389241.2:p.Leu361Ter
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.902T>A
  hgvsp: ENSP00000407747.1:p.Leu301Ter
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.902T>A
  hgvsp: ENSP00000473337.1:p.Leu301Ter
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.902T>A
  hgvsp: ENSP00000407167.2:p.Leu301Ter
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.902T>A
  hgvsp: ENSP00000350154.2:p.Leu301Ter
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.902T>A
  hgvsp: ENSP00000388564.1:p.Leu301Ter
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.902T>A
  hgvsp: ENSP00000316670.4:p.Leu301Ter
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28001
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5694
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu301Ter
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: T
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

2-169952226-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952226
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952224
    reference: chr 2
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1093_1094delTT
  hgvsp: ENSP00000389241.2:p.Leu365IlefsTer10
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.913_914delTT
  hgvsp: ENSP00000473337.1:p.Leu305IlefsTer10
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.913_914delTT
  hgvsp: ENSP00000407747.1:p.Leu305IlefsTer10
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.913_914delTT
  hgvsp: ENSP00000350154.2:p.Leu305IlefsTer10
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.913_914delTT
  hgvsp: ENSP00000407167.2:p.Leu305IlefsTer10
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.913_914delTT
  hgvsp: ENSP00000316670.4:p.Leu305IlefsTer10
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.472_473delTT
  hgvsp: ENSP00000388066.1:p.Leu158IlefsTer10
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.913_914delTT
  hgvsp: ENSP00000388564.1:p.Leu305IlefsTer10
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7933
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1572
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu305IlefsTer10
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: CTT
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

2-169952233-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952233
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952233
    reference: chr 2
allele count: 26826
allele frequency: 2.214060514022548e-1
allele num: 121162
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.916T>C
  hgvsp: ENST00000327239.4:c.916T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.916T>C
  hgvsp: ENST00000412271.1:c.916T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.916T>C
  hgvsp: ENST00000436483.2:c.916T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.916T>C
  hgvsp: ENST00000357546.2:c.916T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.916T>C
  hgvsp: ENST00000428522.1:c.916T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1096T>C
  hgvsp: ENST00000432060.2:c.1096T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.475T>C
  hgvsp: ENST00000421653.1:c.475T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.916T>C
  hgvsp: ENST00000602501.1:c.916T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 878
genotype depth: GenotypeDepth
  all individuals: 8143
  bin: 9.75e1
  variant carriers: 7831
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 3.75e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 3.25e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 19523
  bin: 2.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 2.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 573
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.25e1
  variant carriers: 392
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 7.75e1
  variant carriers: 1933
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 8.75e1
  variant carriers: 1823
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 6.75e1
  variant carriers: 1693
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 9.25e1
  variant carriers: 1575
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 8.25e1
  variant carriers: 1915
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 7.25e1
  variant carriers: 1813
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 6.25e1
  variant carriers: 1445
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 5.75e1
  variant carriers: 1085
genotype quality: GenotypeQuality
  all individuals: 26268
  bin: 6.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 4
hgvs: p.Leu306Leu
num of homozygotes: 3311
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-169952241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 169952241
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 169952241
    reference: chr 2
allele count: 5
allele frequency: 4.129501156260323e-5
allele num: 121080
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000316670
  ensembl transcript: ENST00000327239
  gene symbol: DHRS9
  hgvsc: ENST00000327239.4:c.924A>G
  hgvsp: ENST00000327239.4:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000389241
  ensembl transcript: ENST00000432060
  gene symbol: DHRS9
  hgvsc: ENST00000432060.2:c.1104A>G
  hgvsp: ENST00000432060.2:c.1104A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388564
  ensembl transcript: ENST00000428522
  gene symbol: DHRS9
  hgvsc: ENST00000428522.1:c.924A>G
  hgvsp: ENST00000428522.1:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000350154
  ensembl transcript: ENST00000357546
  gene symbol: DHRS9
  hgvsc: ENST00000357546.2:c.924A>G
  hgvsp: ENST00000357546.2:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000473337
  ensembl transcript: ENST00000602501
  gene symbol: DHRS9
  hgvsc: ENST00000602501.1:c.924A>G
  hgvsp: ENST00000602501.1:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407747
  ensembl transcript: ENST00000412271
  gene symbol: DHRS9
  hgvsc: ENST00000412271.1:c.924A>G
  hgvsp: ENST00000412271.1:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000388066
  ensembl transcript: ENST00000421653
  gene symbol: DHRS9
  hgvsc: ENST00000421653.1:c.483A>G
  hgvsp: ENST00000421653.1:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073737
  ensembl protein: ENSP00000407167
  ensembl transcript: ENST00000436483
  gene symbol: DHRS9
  hgvsc: ENST00000436483.2:c.924A>G
  hgvsp: ENST00000436483.2:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16888
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Lys308Lys
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42237
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7971
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016682252858306e-5
allele num: 66298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.68e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

DP
type: SiteQuality
SIO_000300: 1.710263e6

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.606e1

FS
type: SiteQuality
SIO_000300: 3.274e0

MQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3059
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 502
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66078
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.173984503404555e-4
allele num: 8518
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.535e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

FS
type: SiteQuality
SIO_000300: 2.424e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

DP
type: SiteQuality
SIO_000300: 1.701907e6

QD
type: SiteQuality
SIO_000300: 1.471e1

GenotypeQuality
all individuals: 2126
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7876
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3067
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1913
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51437138443832e-5
allele num: 66034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

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

Latino
type: Population
allele count: 11
allele frequency: 9.638976515948125e-4
allele num: 11412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.700759e6

VQSLOD
type: SiteQuality
SIO_000300: 9.14e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

QD
type: SiteQuality
SIO_000300: 1.352e1

FS
type: SiteQuality
SIO_000300: 1.807e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.88e-1

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2120
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1076
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41266
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65932
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.935458480913026e-4
allele num: 10164
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16324
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.227e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

FS
type: SiteQuality
SIO_000300: 6.919999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.061e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.881e0

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.35e-1

DP
type: SiteQuality
SIO_000300: 1.696862e6

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39616
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3049
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2018
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1818
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7605
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.236746912810279e-5
allele num: 16034
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.968102073365231e-5
allele num: 10032
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65302
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 1.668656e6

QD
type: SiteQuality
SIO_000300: 1.042e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 185
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1724
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7187
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.21036068748487e-4
allele num: 8262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.154e1

DP
type: SiteQuality
SIO_000300: 1.615265e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.128e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.859e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.18e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2043
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.890469416785207e-5
allele num: 11248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64002
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15244
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQ
type: SiteQuality
SIO_000300: 5.811e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.149e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.712e0

DP
type: SiteQuality
SIO_000300: 1.570094e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 1.661e0

QD
type: SiteQuality
SIO_000300: 2.98e0

VQSLOD
type: SiteQuality
SIO_000300: -3.132e0

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.226692836113837e-4
allele num: 8152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

QD
type: SiteQuality
SIO_000300: 6.24e0

DP
type: SiteQuality
SIO_000300: 1.555041e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.381e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 1835
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GenotypeQuality
all individuals: 478
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.92379082634303e-5
allele num: 11206
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.65513110608279e-5
allele num: 15026
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63648
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8096
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.535549e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

FS
type: SiteQuality
SIO_000300: 1.411e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.84e-1

QD
type: SiteQuality
SIO_000300: 1.212e1

GenotypeQuality
all individuals: 753
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 378
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.57143755107172e-5
allele num: 63636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15016
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 1.532554e6

QD
type: SiteQuality
SIO_000300: 8.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.961e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.172e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

GenotypeQuality
all individuals: 2060
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6047
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.57143755107172e-5
allele num: 63636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.172e0

FS
type: SiteQuality
SIO_000300: 3.961e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.532554e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 8.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.68e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 29135
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.73858790080556e-5
allele num: 63310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11176
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.724857213806804e-4
allele num: 8054
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.764069264069264e-5
allele num: 14784
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.71e-1

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.116e0

MQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.501577e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-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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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.484666455896301e-5
allele num: 63260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8030
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.354829968838911e-4
allele num: 14762
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.045806316670153e-4
allele num: 9562
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.89e-1

DP
type: SiteQuality
SIO_000300: 1.491815e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.34e-1

QD
type: SiteQuality
SIO_000300: 1.364e1

FS
type: SiteQuality
SIO_000300: 6.745e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.674e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 1425
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.965393580778196e-5
allele num: 11154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14764
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.4743e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.077e0

MQ
type: SiteQuality
SIO_000300: 6.008e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.24e-1

QD
type: SiteQuality
SIO_000300: 1.429e1

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: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 832
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variant carriers: 0

GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 446
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.25281884239539e-4
allele num: 7982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.591039266849106e-5
allele num: 62852
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.895600606812854e-5
allele num: 14502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11112
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.313e0

DP
type: SiteQuality
SIO_000300: 1.419558e6

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

FS
type: SiteQuality
SIO_000300: 9.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.228e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.122e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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: 5.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 873
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.593523918794021e-5
allele num: 62754
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.398212e6

VQSLOD
type: SiteQuality
SIO_000300: -1.229e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.259e0

ClippingRankSum
type: SiteQuality
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QD
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SIO_000300: 7.19e0

FS
type: SiteQuality
SIO_000300: 2.593e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.02e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.553760099440646e-4
allele num: 6436
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11000
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.243e1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
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SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.094e-1

DP
type: SiteQuality
SIO_000300: 1.28249e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

GenotypeQuality
all individuals: 848
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variant carriers: 0

GenotypeQuality
all individuals: 3000
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 264
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7634
num of homozygotes: 0

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

African
type: Population
allele count: 8
allele frequency: 8.69376222560313e-4
allele num: 9202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10904
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

QD
type: SiteQuality
SIO_000300: 1.596e1

VQSLOD
type: SiteQuality
SIO_000300: 5.03e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.256789e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

GenotypeQuality
all individuals: 5828
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 435
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GenotypeQuality
all individuals: 1546
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9038
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.349522693016245e-5
allele num: 59710
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.87e-1

QD
type: SiteQuality
SIO_000300: 1.588e1

FS
type: SiteQuality
SIO_000300: 3.016e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 1.250099e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 23

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1445
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 21
allele frequency: 1.283932501834189e-3
allele num: 16356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519941634241245e-5
allele num: 65792
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.854989e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.664e0

QD
type: SiteQuality
SIO_000300: 1.377e1

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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bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

South Asian
type: Population
allele count: 16
allele frequency: 9.745401388719698e-4
allele num: 16418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
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: 0
allele frequency: 0.0e0
allele num: 65818
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.352e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

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

DP
type: SiteQuality
SIO_000300: 2.855149e6

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.1020258725897e-5
allele num: 16388
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65802
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.67e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.857281e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.000000000000001e-2

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.949e1

QD
type: SiteQuality
SIO_000300: 1.656e1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517773123273533e-5
allele num: 65886
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -6.639e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.435e0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.215066828675577e-4
allele num: 16460
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
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: 902
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.764e0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

VQSLOD
type: SiteQuality
SIO_000300: -4.883e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.23e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

DP
type: SiteQuality
SIO_000300: 2.870375e6

QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeQuality
all individuals: 5302
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22994
bin: 9.75e1
variant carriers: 7

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.575528014302597e-5
allele num: 66002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.98609731876862e-4
allele num: 10070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 2.877708e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.429e0

FS
type: SiteQuality
SIO_000300: 1.619e0

QD
type: SiteQuality
SIO_000300: 1.349e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25808
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1684
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22996
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5329
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 10078
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514187941007238e-5
allele num: 66042
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.986e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.226e0

VQSLOD
type: SiteQuality
SIO_000300: -1.366e0

QD
type: SiteQuality
SIO_000300: 1.507e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.722e0

FS
type: SiteQuality
SIO_000300: 4.512e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e0

DP
type: SiteQuality
SIO_000300: 2.87912e6

GenotypeQuality
all individuals: 1694
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22999
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1047
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.972775695403433e-4
allele num: 10138
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66130
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -5.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 2.883444e6

QD
type: SiteQuality
SIO_000300: 1.515e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.23e0

FS
type: SiteQuality
SIO_000300: 3.471e0

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1507
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22996
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1044
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66168
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.276437847866419e-4
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.708e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.879e0

MQRankSum
type: SiteQuality
SIO_000300: -5.256e0

MQ
type: SiteQuality
SIO_000300: 5.687e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-2

QD
type: SiteQuality
SIO_000300: 6.85e0

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 2.885149e6

GenotypeQuality
all individuals: 26296
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5399
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1705
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23002
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 447
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66264
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.790483649892304e-5
allele num: 10214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.887898e6

QD
type: SiteQuality
SIO_000300: 4.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.502e0

VQSLOD
type: SiteQuality
SIO_000300: -1.886e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 5.62e1

FS
type: SiteQuality
SIO_000300: 5.112e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.307e0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23002
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1705
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26296
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5399
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66264
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.276437847866419e-4
allele num: 8624
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: 904
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 5.62e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

FS
type: SiteQuality
SIO_000300: 5.112e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.307e0

DP
type: SiteQuality
SIO_000300: 2.887898e6

MQRankSum
type: SiteQuality
SIO_000300: -4.502e0

QD
type: SiteQuality
SIO_000300: 4.17e0

VQSLOD
type: SiteQuality
SIO_000300: -1.886e0

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

GenotypeQuality
all individuals: 26492
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 257
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23025
bin: 9.75e1
variant carriers: 123

GenotypeQuality
all individuals: 444
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 3
allele frequency: 3.31858407079646e-3
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 99
allele frequency: 1.489931673840412e-3
allele num: 66446
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.814333232537043e-3
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.217391304347826e-4
allele num: 11500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

FS
type: SiteQuality
SIO_000300: 1.261e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

DP
type: SiteQuality
SIO_000300: 2.901827e6

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.352e0

QD
type: SiteQuality
SIO_000300: 1.318e1

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

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

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

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

GenotypeQuality
all individuals: 223
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5443
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22935
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26604
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1534
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 9.85e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.625e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.058e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.306e-1

DP
type: SiteQuality
SIO_000300: 2.887458e6

MQRankSum
type: SiteQuality
SIO_000300: 1.91e0

FS
type: SiteQuality
SIO_000300: 3.459e0

GenotypeQuality
all individuals: 26717
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1542
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22938
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1070
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1735
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 5465
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.688097306689835e-5
allele num: 11510
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.889485e6

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.03e1

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

FS
type: SiteQuality
SIO_000300: 1.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-1

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1073
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1545
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5466
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.949e1

MQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

QD
type: SiteQuality
SIO_000300: 1.727e1

FS
type: SiteQuality
SIO_000300: 5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.819e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.75e-2

DP
type: SiteQuality
SIO_000300: 2.890544e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.68e0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1737
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.501935832407936e-5
allele num: 66638
num of homozygotes: 1

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.890544e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.75e-2

MQ
type: SiteQuality
SIO_000300: 5.949e1

QD
type: SiteQuality
SIO_000300: 1.727e1

FS
type: SiteQuality
SIO_000300: 5.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.819e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.68e0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 581
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variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.923076923076923e-4
allele num: 10400
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.719e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.891378e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

QD
type: SiteQuality
SIO_000300: 1.122e1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 2.482e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 7.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 6
allele frequency: 5.212858384013901e-4
allele num: 11510
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 118
allele frequency: 1.134397231301673e-2
allele num: 10402
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

DP
type: SiteQuality
SIO_000300: 2.905872e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.446e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.84e0

MQRankSum
type: SiteQuality
SIO_000300: 5.08e-1

GenotypeQuality
all individuals: 1749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5477
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GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.934e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 2.888182e6

QD
type: SiteQuality
SIO_000300: 1.37e1

MQRankSum
type: SiteQuality
SIO_000300: -7.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.08e-1

MQ
type: SiteQuality
SIO_000300: 5.918e1

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.888518e6

FS
type: SiteQuality
SIO_000300: 8.805e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.33e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.35e0

VQSLOD
type: SiteQuality
SIO_000300: -5.198e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.780346820809249e-4
allele num: 8650
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.889895e6

QD
type: SiteQuality
SIO_000300: 1.264e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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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: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.736714136853074e-4
allele num: 11516
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.889895e6

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.946e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 26845
bin: 6.25e1
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.321e1

MQRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.62e-1

DP
type: SiteQuality
SIO_000300: 2.888544e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.23e-1

FS
type: SiteQuality
SIO_000300: 4.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.0e-3

MQ
type: SiteQuality
SIO_000300: 5.937e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

QD
type: SiteQuality
SIO_000300: 1.449e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 2.888803e6

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 14

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 14
allele frequency: 2.097944014865432e-4
allele num: 66732
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 1.361e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.889909e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 22893
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 7.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.073e0

FS
type: SiteQuality
SIO_000300: 4.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 9.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

DP
type: SiteQuality
SIO_000300: 2.889166e6

GenotypeQuality
all individuals: 22894
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.686587908269631e-5
allele num: 11512
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: 66732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e-1

DP
type: SiteQuality
SIO_000300: 2.889095e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.05e0

QD
type: SiteQuality
SIO_000300: 1.429e1

MQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

FS
type: SiteQuality
SIO_000300: 5.885e0

GenotypeQuality
all individuals: 5489
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.468208092485549e-4
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

FS
type: SiteQuality
SIO_000300: 5.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.457e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

DP
type: SiteQuality
SIO_000300: 2.889575e6

QD
type: SiteQuality
SIO_000300: 1.144e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.889647e6

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 1.731e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 2.88927e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

FS
type: SiteQuality
SIO_000300: 1.144e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

QD
type: SiteQuality
SIO_000300: 1.582e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

MQ
type: SiteQuality
SIO_000300: 5.989e1

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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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 5489
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.04887770086008e-4
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

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

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

Other
type: Population
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allele num: 908
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.504e0

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.889924e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26843
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5489
bin: 6.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.504e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

DP
type: SiteQuality
SIO_000300: 2.889924e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.312e1

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 3.469e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

GenotypeQuality
all individuals: 26845
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22887
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.079e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

QD
type: SiteQuality
SIO_000300: 1.636e1

DP
type: SiteQuality
SIO_000300: 2.888874e6

FS
type: SiteQuality
SIO_000300: 4.142e0

MQRankSum
type: SiteQuality
SIO_000300: -1.422e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-1

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22889
bin: 9.75e1
variant carriers: 2

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

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

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5491
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996973057212216e-5
allele num: 66734
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.003e0

FS
type: SiteQuality
SIO_000300: 9.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e-1

QD
type: SiteQuality
SIO_000300: 1.475e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 2.888903e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5490
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26840
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 583
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.954102920723226e-4
allele num: 11504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 2.731e0

QD
type: SiteQuality
SIO_000300: 1.389e1

DP
type: SiteQuality
SIO_000300: 2.889245e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.054e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 5.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e-1

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

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

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

GenotypeQuality
all individuals: 1758
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22887
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5489
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.1307e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.96e0

DP
type: SiteQuality
SIO_000300: 2.888727e6

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.395e0

QD
type: SiteQuality
SIO_000300: 1.572e1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.14e-1

GenotypeQuality
all individuals: 1072
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26835
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22886
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 5488
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 583
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.798183834327329e-4
allele num: 66734
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.888675e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.41e0

FS
type: SiteQuality
SIO_000300: 1.199e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

QD
type: SiteQuality
SIO_000300: 1.427e1

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
SIO_000300: 3.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.26e-1

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

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1545
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5487
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22892
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 583
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
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: 10
allele frequency: 6.056201550387597e-4
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 2.889454e6

QD
type: SiteQuality
SIO_000300: 1.321e1

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 23283
bin: 9.75e1
variant carriers: 2233

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 426
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 10
allele frequency: 9.611687812379854e-4
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 93
allele frequency: 1.39359247160368e-3
allele num: 66734
num of homozygotes: 0

Latino
type: Population
allele count: 377
allele frequency: 3.276551364505476e-2
allele num: 11506
num of homozygotes: 7

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 1111
allele frequency: 1.285582041194168e-1
allele num: 8642
num of homozygotes: 73

South Asian
type: Population
allele count: 725
allele frequency: 4.390746124031008e-2
allele num: 16512
num of homozygotes: 17

Other
type: Population
allele count: 14
allele frequency: 1.541850220264317e-2
allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.42e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.84e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.419999999999999e-2

DP
type: SiteQuality
SIO_000300: 3.04003e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.067e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

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

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

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

GenotypeQuality
all individuals: 21685
bin: 9.75e1
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GenotypeQuality
all individuals: 574
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 1057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.697e0

DP
type: SiteQuality
SIO_000300: 2.822503e6

QD
type: SiteQuality
SIO_000300: 1.413e1

MQ
type: SiteQuality
SIO_000300: 5.939e1

MQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 5.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e-1

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 572
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21741
bin: 9.75e1
variant carriers: 461

GenotypeQuality
all individuals: 1053
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5669
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 7.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 31
allele frequency: 4.68702751738736e-3
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 30
allele frequency: 2.608242044861763e-3
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 364
allele frequency: 5.454490964126232e-3
allele num: 66734
num of homozygotes: 1

African
type: Population
allele count: 5
allele frequency: 4.804920238324044e-4
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.607929515418502e-3
allele num: 908
num of homozygotes: 0

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

South Asian
type: Population
allele count: 26
allele frequency: 1.574612403100775e-3
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.65e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.14e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

QD
type: SiteQuality
SIO_000300: 1.519e1

DP
type: SiteQuality
SIO_000300: 2.846611e6

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21402
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1784
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 28069
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 8.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.803352e6

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.05e-1

FS
type: SiteQuality
SIO_000300: 6.15e0

QD
type: SiteQuality
SIO_000300: 1.084e1

VQSLOD
type: SiteQuality
SIO_000300: 5.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

GenotypeQuality
all individuals: 1579
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5716
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21401
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 4.898e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

DP
type: SiteQuality
SIO_000300: 2.803003e6

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e0

QD
type: SiteQuality
SIO_000300: 1.376e1

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

GenotypeQuality
all individuals: 49
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21401
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5716
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1579
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28050
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

FS
type: SiteQuality
SIO_000300: 4.898e0

DP
type: SiteQuality
SIO_000300: 2.803003e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.376e1

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

GenotypeQuality
all individuals: 1786
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5716
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28042
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 21401
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

DP
type: SiteQuality
SIO_000300: 2.802833e6

FS
type: SiteQuality
SIO_000300: 7.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.586e1

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21402
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5704
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1782
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.25e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

DP
type: SiteQuality
SIO_000300: 2.802527e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.05e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

FS
type: SiteQuality
SIO_000300: 7.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

GenotypeQuality
all individuals: 21402
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5701
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28040
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 9.25e1
variant carriers: 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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

QD
type: SiteQuality
SIO_000300: 9.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.767e0

FS
type: SiteQuality
SIO_000300: 6.046e0

VQSLOD
type: SiteQuality
SIO_000300: 3.03e-1

DP
type: SiteQuality
SIO_000300: 2.802543e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

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

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

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

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

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

GenotypeQuality
all individuals: 5701
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21402
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28040
bin: 6.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

DP
type: SiteQuality
SIO_000300: 2.802543e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.767e0

VQSLOD
type: SiteQuality
SIO_000300: 3.03e-1

FS
type: SiteQuality
SIO_000300: 6.046e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.63e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

QD
type: SiteQuality
SIO_000300: 9.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

GenotypeQuality
all individuals: 67
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 575
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21402
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 7.25e1
variant carriers: 0

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

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

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

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: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

DP
type: SiteQuality
SIO_000300: 2.801855e6

QD
type: SiteQuality
SIO_000300: 1.408e1

FS
type: SiteQuality
SIO_000300: 4.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.586e0

VQSLOD
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

GenotypeQuality
all individuals: 5693
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21401
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27966
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1056
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1782
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 2.801432e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e-1

QD
type: SiteQuality
SIO_000300: 1.793e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.014e0

MQ
type: SiteQuality
SIO_000300: 6.046e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 4.69e0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1409
bin: 7.75e1
variant carriers: 7

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 335
bin: 9.25e1
variant carriers: 16

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 280
bin: 8.75e1
variant carriers: 17

GenotypeQuality
all individuals: 728
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 24978
bin: 9.75e1
variant carriers: 23430

GenotypeQuality
all individuals: 5115
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1305
bin: 7.25e1
variant carriers: 8

South Asian
type: Population
allele count: 2753
allele frequency: 1.667676278168161e-1
allele num: 16508
num of homozygotes: 230

East Asian
type: Population
allele count: 2738
allele frequency: 3.182240818224082e-1
allele num: 8604
num of homozygotes: 434

African
type: Population
allele count: 3946
allele frequency: 3.794960569340258e-1
allele num: 10398
num of homozygotes: 783

Other
type: Population
allele count: 219
allele frequency: 2.411894273127753e-1
allele num: 908
num of homozygotes: 27

European (Finnish)
type: Population
allele count: 1147
allele frequency: 1.736826165960024e-1
allele num: 6604
num of homozygotes: 87

European (Non-Finnish)
type: Population
allele count: 13094
allele frequency: 1.963530576132921e-1
allele num: 66686
num of homozygotes: 1349

Latino
type: Population
allele count: 2929
allele frequency: 2.557185262790291e-1
allele num: 11454
num of homozygotes: 401

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

DP
type: SiteQuality
SIO_000300: 3.165434e6

QD
type: SiteQuality
SIO_000300: 1.816e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.11e-2