14-24114490-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114490
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114490
    reference: chr 14
allele count: 1
allele frequency: 8.285416010737898e-6
allele num: 120694
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2237G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4960G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2801G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451485
  ensembl transcript: ENST00000553600
  gene symbol: DHRS2
  hgvsc: ENST00000553600.1:c.*344G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*28G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.882G>C
  hgvsp: ENST00000344777.7:c.882G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*28G>C
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val294Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

14-24114491-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114491
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114491
    reference: chr 14
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2802G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451485
  ensembl transcript: ENST00000553600
  gene symbol: DHRS2
  hgvsc: ENST00000553600.1:c.*345G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4961G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.883G>A
  hgvsp: ENSP00000344674.7:p.Val295Ile
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*29G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2238G>A
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1627
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val295Ile
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

14-24114493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114493
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114493
    reference: chr 14
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*31C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.885C>T
  hgvsp: ENST00000344777.7:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451485
  ensembl transcript: ENST00000553600
  gene symbol: DHRS2
  hgvsc: ENST00000553600.1:c.*347C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*31C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2804C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2240C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4963C>T
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7876
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1358
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 983
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val295Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

14-24114496-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114496
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114496
    reference: chr 14
allele count: 1
allele frequency: 8.310755780130645e-6
allele num: 120326
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.888A>G
  hgvsp: ENST00000344777.7:c.888A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2807A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4966A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451485
  ensembl transcript: ENST00000553600
  gene symbol: DHRS2
  hgvsc: ENST00000553600.1:c.*350A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*34A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*34A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2243A>G
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2304
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7897
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro296Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

14-24114500-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114500
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114500
    reference: chr 14
allele count: 6
allele frequency: 4.996835337619508e-5
allele num: 120076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2247C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.892C>T
  hgvsp: ENSP00000344674.7:p.Pro298Ser
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*38C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2811C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4970C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451485
  ensembl transcript: ENST00000553600
  gene symbol: DHRS2
  hgvsc: ENST00000553600.1:c.*354C>T
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7639
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro298Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/14-24114502-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114502
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114502
    reference: chr 14
allele count: 1
allele frequency: 8.340700952508049e-6
allele num: 119894
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4972A>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*40A>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451485
  ensembl transcript: ENST00000553600
  gene symbol: DHRS2
  hgvsc: ENST00000553600.1:c.*356A>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2813A>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2249A>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*40A>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.894A>C
  hgvsp: ENST00000344777.7:c.894A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7341
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2184
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro298Pro
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/14-24114508-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114508
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114508
    reference: chr 14
allele count: 1
allele frequency: 8.353660574063554e-6
allele num: 119708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2819C>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2255C>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4978C>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.900C>A
  hgvsp: ENST00000344777.7:c.900C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*46C>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*46C>A
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7196
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala300Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

14-24114508-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114508
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114508
    reference: chr 14
allele count: 3
allele frequency: 2.506098172219066e-5
allele num: 119708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*46C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4978C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*46C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.900C>T
  hgvsp: ENST00000344777.7:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2255C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2819C>T
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42346
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala300Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

14-24114511-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114511
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114512
    reference: chr 14
allele count: 1
allele frequency: 8.363161944267889e-6
allele num: 119572
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2827dupG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2263dupG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*54dupG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*54dupG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4986dupG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*5dupG
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7086
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2124
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42340
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1797
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

14-24114511-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114511
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114511
    reference: chr 14
allele count: 6
allele frequency: 5.017897166560734e-5
allele num: 119572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*49A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2822A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2258A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*49A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.903A>G
  hgvsp: ENSP00000344674.7:p.Ter301TrpextTer4
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4981A>G
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2124
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7086
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1797
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ter301TrpextTer4
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

14-24114515-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114515
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114515
    reference: chr 14
allele count: 3
allele frequency: 2.516018652084941e-5
allele num: 119236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*53G>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*4G>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4985G>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*53G>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2826G>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2262G>T
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1337
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

14-24114515-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114515
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114515
    reference: chr 14
allele count: 1
allele frequency: 8.386728840283135e-6
allele num: 119236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2826G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*53G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*53G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*4G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4985G>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2262G>C
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6640
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1337
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

14-24114521-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114521
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114521
    reference: chr 14
allele count: 1
allele frequency: 8.403643819960336e-6
allele num: 118996
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*59T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*10T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2268T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*59T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4991T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2832T>G
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42339
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 893
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-24114527-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114527
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114527
    reference: chr 14
allele count: 1
allele frequency: 8.430992327796981e-6
allele num: 118610
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*65A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2838A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2274A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*65A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.4997A>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*16A>G
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 915
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6083
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

14-24114532-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114532
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114532
    reference: chr 14
allele count: 3
allele frequency: 2.532714225411566e-5
allele num: 118450
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*21T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2843T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*70T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*70T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.5002T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2279T>C
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42338
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5926
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

14-24114544-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114544
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114544
    reference: chr 14
allele count: 1
allele frequency: 8.489829184636805e-6
allele num: 117788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*82G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*33G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2291G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*82G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2855G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.5014G>A
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42335
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1304
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4549
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-24114545-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114545
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114543
    reference: chr 14
allele count: 1
allele frequency: 8.499498529586754e-6
allele num: 117654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2859_2860delAG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.5018_5019delAG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*86_*87delAG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*37_*38delAG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*86_*87delAG
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2295_2296delAG
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1810
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: CAG
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

14-24114550-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114550
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114550
    reference: chr 14
allele count: 2
allele frequency: 1.709343270315545e-5
allele num: 117004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*88T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2297T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*39T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2861T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*88T>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.5020T>G
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1371
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-24114551-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114551
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114551
    reference: chr 14
allele count: 1
allele frequency: 8.545547769612032e-6
allele num: 117020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2298C>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*40C>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*89C>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*89C>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2862C>G
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.5021C>G
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3388
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

14-24114551-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114551
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114551
    reference: chr 14
allele count: 1
allele frequency: 8.545547769612032e-6
allele num: 117020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*89C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2862C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*40C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*89C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2298C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.5021C>T
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42332
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-24114553-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114553
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114553
    reference: chr 14
allele count: 1
allele frequency: 8.547300762419228e-6
allele num: 116996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*91G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2864G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*91G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.5023G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*42G>A
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2300G>A
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1464
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42329
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

14-24114560-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114560
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114560
    reference: chr 14
allele count: 3
allele frequency: 2.567789646672144e-5
allele num: 116832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*98T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.5030T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2307T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*98T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*49T>C
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2871T>C
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4866
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42325
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

14-24114563-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24114563
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24114563
    reference: chr 14
allele count: 3
allele frequency: 2.572236988767898e-5
allele num: 116630
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000250383
  ensembl transcript: ENST00000250383
  gene symbol: DHRS2
  hgvsc: ENST00000250383.6:c.*101C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556701
  gene symbol: DHRS2
  hgvsc: ENST00000556701.1:n.2874C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556550
  gene symbol: DHRS2
  hgvsc: ENST00000556550.1:n.2310C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100867
  ensembl transcript: ENST00000556729
  gene symbol: DHRS2
  hgvsc: ENST00000556729.1:n.5033C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000451895
  ensembl transcript: ENST00000557535
  gene symbol: DHRS2
  hgvsc: ENST00000557535.1:c.*101C>T
  variant of: http://identifiers.org/hgnc/18349
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000100867
  ensembl protein: ENSP00000344674
  ensembl transcript: ENST00000344777
  gene symbol: DHRS2
  hgvsc: ENST00000344777.7:c.*52C>T
  variant of: http://identifiers.org/hgnc/18349
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2421
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42330
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

14-24408702-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408702
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408702
    reference: chr 14
allele count: 1
allele frequency: 7.077140835102619e-5
allele num: 14130
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.-32G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.2090C>T
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4651
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 180
  num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

14-24408750-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408750
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408750
    reference: chr 14
allele count: 14
allele frequency: 9.934714731762702e-4
allele num: 14092
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.17T>C
  hgvsp: ENSP00000346918.1:p.Ile6Thr
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.2042A>G
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 2.5e0
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genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
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genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 5567
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
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  variant carriers: 0
hgvs: p.Ile6Thr
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 180
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

14-24408752-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408752
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408752
    reference: chr 14
allele count: 1
allele frequency: 7.106310403638431e-5
allele num: 14072
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.19T>G
  hgvsp: ENSP00000346918.1:p.Cys7Gly
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.2040A>C
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5570
  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
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  variant carriers: 0
hgvs: p.Cys7Gly
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1598
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

14-24408839-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408839
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408839
    reference: chr 14
allele count: 1
allele frequency: 7.850525985241011e-5
allele num: 12738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.1953C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.1831C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.106G>C
  hgvsp: ENSP00000346918.1:p.Ala36Pro
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 730
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 19
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala36Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

14-24408856-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408856
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408856
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 12426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.1936C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.123G>C
  hgvsp: ENSP00000346918.1:p.Glu41Asp
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.1814C>G
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4765
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2537
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu41Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

14-24408866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408866
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408866
    reference: chr 14
allele count: 721
allele frequency: 5.930251686132588e-2
allele num: 12158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.1926C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.133G>A
  hgvsp: ENSP00000346918.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.1804C>T
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 3.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 2.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 2.5e0
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 7.5e0
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 9.75e1
  variant carriers: 664
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 2.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 7.5e0
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 6.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4264
  bin: 6.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.75e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 9.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala45Thr
num of homozygotes: 50
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum

14-24408879-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408879
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408879
    reference: chr 14
allele count: 336
allele frequency: 2.916160388821385e-2
allele num: 11522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.1791T>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.146A>G
  hgvsp: ENSP00000346918.1:p.Asn49Ser
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.1913T>C
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 2.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 7.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 9.75e1
  variant carriers: 322
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4114
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn49Ser
num of homozygotes: 9
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

14-24408929-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408929
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408929
    reference: chr 14
allele count: 1
allele frequency: 1.715854495538778e-4
allele num: 5828
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.1863A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.1741A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.196T>C
  hgvsp: ENSP00000346918.1:p.Ter66GlnextTer45
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3343
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4085
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ter66GlnextTer45
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

14-24408930-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408930
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408930
    reference: chr 14
allele count: 1
allele frequency: 1.764290755116443e-4
allele num: 5668
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.1862T>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.197A>G
  hgvsp: ENSP00000346918.1:p.Ter66TrpextTer45
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.1740T>C
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4008
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3362
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ter66TrpextTer45
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

14-24408954-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24408954
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24408954
    reference: chr 14
allele count: 391
allele frequency: 1.606409202958094e-1
allele num: 2434
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000197775
  ensembl protein: ENSP00000346918
  ensembl transcript: ENST00000354854
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000354854.1:c.*23A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.1838T>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.1716T>C
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 2.5e0
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 7.5e0
  variant carriers: 555
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 1.25e1
  variant carriers: 293
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 1.75e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 3838
  bin: 7.5e0
  variant carriers: 84
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 2.25e1
  variant carriers: 51
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 8.75e1
  variant carriers: 49
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 1.25e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.75e1
  variant carriers: 43
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 9.75e1
  variant carriers: 361
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 6.25e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 8.25e1
  variant carriers: 83
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 18
num of homozygotes: 31
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

14-24422955-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422955
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422955
    reference: chr 14
allele count: 1
allele frequency: 8.32279113123377e-6
allele num: 120152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.79+28G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.424+28G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.302+28G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-43C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.377G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12588G>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25630
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2511
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33588
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/14-24422956-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422956
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422956
    reference: chr 14
allele count: 2
allele frequency: 1.665667266306883e-5
allele num: 120072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12589G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.424+27G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.79+27G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-42C>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.302+27G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.376G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-42C>A
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25699
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2478
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33771
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

14-24422956-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422956
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422956
    reference: chr 14
allele count: 12
allele frequency: 9.994003597841295e-5
allele num: 120072
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-42C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12589G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-42C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.376G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.79+27G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.302+27G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.424+27G>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12385
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8958
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

14-24422969-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422969
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422969
    reference: chr 14
allele count: 2
allele frequency: 1.661681621801263e-5
allele num: 120360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-29A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.79+14T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-29A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.302+14T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.363T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12602T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.424+14T>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35925
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2614
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/14-24422978-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422978
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422978
    reference: chr 14
allele count: 2
allele frequency: 1.659255326209597e-5
allele num: 120536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.79+5G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.302+5G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-20C>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12611G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.354G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.424+5G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-20C>A
  variant of: http://identifiers.org/hgnc/16985
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
hgvs: n.79+5G>T
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

14-24422980-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422980
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422980
    reference: chr 14
allele count: 2
allele frequency: 1.658539821541115e-5
allele num: 120588
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.-18T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-72T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.302+3A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-18T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.79+3A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.352A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-72T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.424+3A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-72T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-18T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12613A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-72T>G
  variant of: http://identifiers.org/hgnc/16985
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.79+3A>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

14-24422981-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422981
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422981
    reference: chr 14
allele count: 1
allele frequency: 8.290499088045101e-6
allele num: 120620
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-17A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-17A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-71A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.424+2T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.-17A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.302+2T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-71A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.79+2T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-71A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-71A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.351T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12614T>A
  variant of: http://identifiers.org/hgnc/23175
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.79+2T>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

14-24422989-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422989
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422989
    reference: chr 14
allele count: 5
allele frequency: 4.141953013685013e-5
allele num: 120716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-9G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-63G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-63G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.343C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-9G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-63G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-63G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.73C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.296C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.-9G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12622C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.-9G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.418C>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26705
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

14-24422991-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422991
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422991
    reference: chr 14
allele count: 982
allele frequency: 8.133717655633966e-3
allele num: 120732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-7C>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12624G>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-7C>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.416G>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.294G>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-61C>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.-7C>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-61C>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.341G>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-61C>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.71G>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.-7C>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-61C>G
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 4.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 6.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 12518
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 26695
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 11904
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 3.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 4.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 134
genotype quality: GenotypeQuality
num of homozygotes: 4
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

14-24422993-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422993
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422993
    reference: chr 14
allele count: 6
allele frequency: 4.969108707534825e-5
allele num: 120746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-5G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-5G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-59G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.292C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-59G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.-5G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12626C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-59G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-59G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.-5G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.339C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.69C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.414C>G
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

14-24422995-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422995
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422995
    reference: chr 14
allele count: 10589
allele frequency: 8.766018742342462e-2
allele num: 120796
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-57T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.-3T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.-3T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-3T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-57T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.290A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.412A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.-3T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-57T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12628A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-3T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-57T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.337A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.67A>C
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 5.25e1
  variant carriers: 846
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 12078
  bin: 3.25e1
  variant carriers: 726
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.75e1
  variant carriers: 1003
genotype depth: GenotypeDepth
  all individuals: 26359
  bin: 2.75e1
  variant carriers: 471
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 628
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 348
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 2.25e1
  variant carriers: 295
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 3.75e1
  variant carriers: 939
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 457
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1698
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum

14-24422996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422996
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422996
    reference: chr 14
allele count: 1
allele frequency: 8.272940865018697e-6
allele num: 120876
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.336G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-56C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.411G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.-2C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12629G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-56C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.-2C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.-2C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.-2C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.-2C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-56C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.66G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-56C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.289G>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

14-24422999-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24422999
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24422999
    reference: chr 14
allele count: 1
allele frequency: 8.272530236098013e-6
allele num: 120882
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.2T>C
  hgvsp: ENSP00000452645.1:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.2T>C
  hgvsp: ENSP00000326219.5:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-53T>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.2T>C
  hgvsp: ENSP00000380264.3:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.2T>C
  hgvsp: ENSP00000453367.1:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.333A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-53T>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.2T>C
  hgvsp: ENSP00000440508.2:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.63A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.2T>C
  hgvsp: ENSP00000380265.3:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.2T>C
  hgvsp: ENSP00000453983.1:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.408A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.286A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12632A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-53T>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-53T>C
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: start lost
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26551
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS

14-24423002-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423002
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423002
    reference: chr 14
allele count: 47
allele frequency: 3.88853956382169e-4
allele num: 120868
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-50A>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.5A>G
  hgvsp: ENSP00000453367.1:p.His2Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.5A>G
  hgvsp: ENSP00000326219.5:p.His2Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.5A>G
  hgvsp: ENSP00000380265.3:p.His2Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.5A>G
  hgvsp: ENSP00000453983.1:p.His2Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.60T>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-50A>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.330T>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12635T>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.5A>G
  hgvsp: ENSP00000380264.3:p.His2Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.5A>G
  hgvsp: ENSP00000452645.1:p.His2Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.5A>G
  hgvsp: ENSP00000440508.2:p.His2Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-50A>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.405T>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-50A>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.283T>C
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His2Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

14-24423003-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423003
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423003
    reference: chr 14
allele count: 1
allele frequency: 8.274583788435442e-6
allele num: 120852
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.329G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12636G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.6C>T
  hgvsp: ENST00000397075.3:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.404G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-49C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.6C>T
  hgvsp: ENST00000397074.3:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.6C>T
  hgvsp: ENST00000559632.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.6C>T
  hgvsp: ENST00000558263.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.282G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-49C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.6C>T
  hgvsp: ENST00000313250.5:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.6C>T
  hgvsp: ENST00000558581.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.59G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.6C>T
  hgvsp: ENST00000543741.2:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-49C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-49C>T
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His2His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

14-24423005-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423005
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423005
    reference: chr 14
allele count: 10
allele frequency: 8.27417299640901e-5
allele num: 120858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.8A>T
  hgvsp: ENSP00000452645.1:p.Lys3Met
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.8A>T
  hgvsp: ENSP00000453983.1:p.Lys3Met
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-47A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.8A>T
  hgvsp: ENSP00000380265.3:p.Lys3Met
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.8A>T
  hgvsp: ENSP00000326219.5:p.Lys3Met
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.8A>T
  hgvsp: ENSP00000380264.3:p.Lys3Met
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.8A>T
  hgvsp: ENSP00000453367.1:p.Lys3Met
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-47A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.280T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.8A>T
  hgvsp: ENSP00000440508.2:p.Lys3Met
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.327T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.402T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12638T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-47A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-47A>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.57T>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Lys3Met
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

14-24423006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423006
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423006
    reference: chr 14
allele count: 1
allele frequency: 8.276090374906894e-6
allele num: 120830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.9G>A
  hgvsp: ENST00000543741.2:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.9G>A
  hgvsp: ENST00000397074.3:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.9G>A
  hgvsp: ENST00000558581.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-46G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-46G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.326C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.9G>A
  hgvsp: ENST00000313250.5:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-46G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.56C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.9G>A
  hgvsp: ENST00000559632.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.9G>A
  hgvsp: ENST00000397075.3:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.9G>A
  hgvsp: ENST00000558263.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12639C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.279C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.401C>T
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys3Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

14-24423007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423007
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423007
    reference: chr 14
allele count: 10557
allele frequency: 8.744160620216679e-2
allele num: 120732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.10G>A
  hgvsp: ENSP00000453367.1:p.Ala4Thr
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-45G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.10G>A
  hgvsp: ENSP00000452645.1:p.Ala4Thr
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.400C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.10G>A
  hgvsp: ENSP00000440508.2:p.Ala4Thr
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.325C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.10G>A
  hgvsp: ENSP00000380265.3:p.Ala4Thr
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.55C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.10G>A
  hgvsp: ENSP00000453983.1:p.Ala4Thr
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-45G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-45G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.10G>A
  hgvsp: ENSP00000380264.3:p.Ala4Thr
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-45G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12640C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.10G>A
  hgvsp: ENSP00000326219.5:p.Ala4Thr
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.278C>T
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10844
  bin: 2.25e1
  variant carriers: 334
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 4.75e1
  variant carriers: 1013
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 4.25e1
  variant carriers: 1031
genotype depth: GenotypeDepth
  all individuals: 26478
  bin: 2.75e1
  variant carriers: 529
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 6.25e1
  variant carriers: 581
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 456
genotype quality: GenotypeQuality
hgvs: p.Ala4Thr
num of homozygotes: 1681
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-24423009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423009
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423009
    reference: chr 14
allele count: 2
allele frequency: 1.659558225600345e-5
allele num: 120514
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.323C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.12G>A
  hgvsp: ENST00000397075.3:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.53C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.12G>A
  hgvsp: ENST00000543741.2:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.276C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-43G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.12G>A
  hgvsp: ENST00000397074.3:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-43G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.12G>A
  hgvsp: ENST00000558581.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.12G>A
  hgvsp: ENST00000559632.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-43G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.12G>A
  hgvsp: ENST00000313250.5:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.12G>A
  hgvsp: ENST00000558263.1:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12642C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.398C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-43G>A
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala4Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

14-24423009-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423009
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423009
    reference: chr 14
allele count: 12
allele frequency: 9.957349353602072e-5
allele num: 120514
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.276C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.12G>C
  hgvsp: ENST00000558581.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.398C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-43G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.53C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.12G>C
  hgvsp: ENST00000558263.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.323C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-43G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-43G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.12G>C
  hgvsp: ENST00000397075.3:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.12G>C
  hgvsp: ENST00000543741.2:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.12G>C
  hgvsp: ENST00000397074.3:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.12G>C
  hgvsp: ENST00000559632.1:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12642C>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-43G>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.12G>C
  hgvsp: ENST00000313250.5:c.12G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala4Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

14-24423010-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423010
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423010
    reference: chr 14
allele count: 10
allele frequency: 8.297515723792297e-5
allele num: 120518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12643C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.397C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.275C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.52C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-42G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.322C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.13G>A
  hgvsp: ENSP00000380264.3:p.Gly5Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-42G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-42G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.13G>A
  hgvsp: ENSP00000380265.3:p.Gly5Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.13G>A
  hgvsp: ENSP00000453983.1:p.Gly5Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.13G>A
  hgvsp: ENSP00000326219.5:p.Gly5Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-42G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.13G>A
  hgvsp: ENSP00000453367.1:p.Gly5Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.13G>A
  hgvsp: ENSP00000440508.2:p.Gly5Arg
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.13G>A
  hgvsp: ENSP00000452645.1:p.Gly5Arg
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly5Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-24423010-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423010
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423010
    reference: chr 14
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12643C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-42G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.275C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-42G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.13G>T
  hgvsp: ENSP00000453983.1:p.Gly5Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.13G>T
  hgvsp: ENSP00000453367.1:p.Gly5Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.13G>T
  hgvsp: ENSP00000326219.5:p.Gly5Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.322C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.13G>T
  hgvsp: ENSP00000380265.3:p.Gly5Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.13G>T
  hgvsp: ENSP00000440508.2:p.Gly5Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-42G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.13G>T
  hgvsp: ENSP00000380264.3:p.Gly5Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.13G>T
  hgvsp: ENSP00000452645.1:p.Gly5Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.52C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.397C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-42G>T
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly5Trp
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

14-24423022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423022
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423022
    reference: chr 14
allele count: 1
allele frequency: 8.3301401129567e-6
allele num: 120046
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.25C>T
  hgvsp: ENSP00000440508.2:p.Leu9Phe
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.25C>T
  hgvsp: ENSP00000453367.1:p.Leu9Phe
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.25C>T
  hgvsp: ENSP00000452645.1:p.Leu9Phe
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.25C>T
  hgvsp: ENSP00000380264.3:p.Leu9Phe
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.40G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.25C>T
  hgvsp: ENSP00000453983.1:p.Leu9Phe
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.25C>T
  hgvsp: ENSP00000326219.5:p.Leu9Phe
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-30C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-30C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-30C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.25C>T
  hgvsp: ENSP00000380265.3:p.Leu9Phe
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.310G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-30C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.385G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.263G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12655G>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu9Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

14-24423023-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423023
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423023
    reference: chr 14
allele count: 18
allele frequency: 1.500400106695119e-4
allele num: 119968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.26T>C
  hgvsp: ENSP00000380264.3:p.Leu9Pro
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.26T>C
  hgvsp: ENSP00000453983.1:p.Leu9Pro
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-29T>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.26T>C
  hgvsp: ENSP00000453367.1:p.Leu9Pro
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-29T>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.26T>C
  hgvsp: ENSP00000380265.3:p.Leu9Pro
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12656A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.262A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-29T>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.26T>C
  hgvsp: ENSP00000440508.2:p.Leu9Pro
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-29T>C
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.26T>C
  hgvsp: ENSP00000326219.5:p.Leu9Pro
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.309A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.26T>C
  hgvsp: ENSP00000452645.1:p.Leu9Pro
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.384A>G
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.39A>G
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu9Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

14-24423030-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423030
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423030
    reference: chr 14
allele count: 1
allele frequency: 8.377735330585436e-6
allele num: 119364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.33C>T
  hgvsp: ENST00000559632.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-22C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.32G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.33C>T
  hgvsp: ENST00000397074.3:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.33C>T
  hgvsp: ENST00000558581.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.33C>T
  hgvsp: ENST00000543741.2:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.377G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.33C>T
  hgvsp: ENST00000313250.5:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.302G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.33C>T
  hgvsp: ENST00000397075.3:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-22C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-22C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.255G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.33C>T
  hgvsp: ENST00000558263.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12663G>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala11Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-24423031-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423031
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423031
    reference: chr 14
allele count: 171
allele frequency: 1.434130631688416e-3
allele num: 119236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.34C>A
  hgvsp: ENST00000558263.1:c.34C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12664G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-21C>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.34C>A
  hgvsp: ENST00000543741.2:c.34C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.34C>A
  hgvsp: ENST00000397074.3:c.34C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-21C>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.34C>A
  hgvsp: ENST00000313250.5:c.34C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-21C>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.34C>A
  hgvsp: ENST00000558581.1:c.34C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.34C>A
  hgvsp: ENST00000397075.3:c.34C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-21C>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.376G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.34C>A
  hgvsp: ENST00000559632.1:c.34C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.301G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.254G>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.31G>T
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 2.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 28644
  bin: 2.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
hgvs: p.Arg12Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

14-24423031-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423031
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423031
    reference: chr 14
allele count: 1
allele frequency: 8.386728840283135e-6
allele num: 119236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-21C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.34C>T
  hgvsp: ENSP00000453367.1:p.Arg12Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.34C>T
  hgvsp: ENSP00000452645.1:p.Arg12Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-21C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.34C>T
  hgvsp: ENSP00000326219.5:p.Arg12Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-21C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.301G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.31G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.376G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.34C>T
  hgvsp: ENSP00000380265.3:p.Arg12Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.34C>T
  hgvsp: ENSP00000440508.2:p.Arg12Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.34C>T
  hgvsp: ENSP00000380264.3:p.Arg12Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.34C>T
  hgvsp: ENSP00000453983.1:p.Arg12Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12664G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.254G>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg12Trp
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

14-24423033-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423033
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423033
    reference: chr 14
allele count: 1
allele frequency: 8.396446623788812e-6
allele num: 119098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.36G>A
  hgvsp: ENST00000543741.2:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-19G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.36G>A
  hgvsp: ENST00000313250.5:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.374C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.36G>A
  hgvsp: ENST00000397075.3:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.299C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.36G>A
  hgvsp: ENST00000558581.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-19G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.36G>A
  hgvsp: ENST00000558263.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-19G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.36G>A
  hgvsp: ENST00000397074.3:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.252C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.36G>A
  hgvsp: ENST00000559632.1:c.36G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12666C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-19G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.29C>T
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg12Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

14-24423038-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423038
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423038
    reference: chr 14
allele count: 1
allele frequency: 8.462814393554721e-6
allele num: 118164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-14G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-14G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-14G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.41G>T
  hgvsp: ENSP00000380264.3:p.Trp14Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.41G>T
  hgvsp: ENSP00000452645.1:p.Trp14Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-14G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.41G>T
  hgvsp: ENSP00000453367.1:p.Trp14Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.41G>T
  hgvsp: ENSP00000326219.5:p.Trp14Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.41G>T
  hgvsp: ENSP00000380265.3:p.Trp14Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12671C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.24C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.369C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.41G>T
  hgvsp: ENSP00000453983.1:p.Trp14Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.41G>T
  hgvsp: ENSP00000440508.2:p.Trp14Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.247C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.294C>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27589
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp14Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

14-24423039-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423039
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423039
    reference: chr 14
allele count: 2
allele frequency: 1.692763436309776e-5
allele num: 118150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.368C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.246C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.42G>A
  hgvsp: ENSP00000440508.2:p.Trp14Ter
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.42G>A
  hgvsp: ENSP00000380264.3:p.Trp14Ter
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-13G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-13G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.23C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.42G>A
  hgvsp: ENSP00000326219.5:p.Trp14Ter
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-13G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.42G>A
  hgvsp: ENSP00000380265.3:p.Trp14Ter
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.42G>A
  hgvsp: ENSP00000452645.1:p.Trp14Ter
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.42G>A
  hgvsp: ENSP00000453367.1:p.Trp14Ter
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.42G>A
  hgvsp: ENSP00000453983.1:p.Trp14Ter
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.293C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-13G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12672C>T
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp14Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

14-24423042-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423042
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423042
    reference: chr 14
allele count: 6
allele frequency: 5.103603143819537e-5
allele num: 117564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-10T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12675A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-10T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.45T>G
  hgvsp: ENSP00000380265.3:p.Asn15Lys
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.290A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.20A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.45T>G
  hgvsp: ENSP00000452645.1:p.Asn15Lys
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.45T>G
  hgvsp: ENSP00000453983.1:p.Asn15Lys
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.243A>C
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.45T>G
  hgvsp: ENSP00000440508.2:p.Asn15Lys
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.45T>G
  hgvsp: ENSP00000326219.5:p.Asn15Lys
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-10T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-10T>G
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.45T>G
  hgvsp: ENSP00000380264.3:p.Asn15Lys
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.45T>G
  hgvsp: ENSP00000453367.1:p.Asn15Lys
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.365A>C
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn15Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

14-24423044-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423044
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423044
    reference: chr 14
allele count: 1
allele frequency: 8.543795495711015e-6
allele num: 117044
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.47C>T
  hgvsp: ENSP00000326219.5:p.Ser16Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-8C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.47C>T
  hgvsp: ENSP00000453367.1:p.Ser16Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.18G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.288G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-8C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12677G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.47C>T
  hgvsp: ENSP00000452645.1:p.Ser16Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.47C>T
  hgvsp: ENSP00000380265.3:p.Ser16Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.363G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.47C>T
  hgvsp: ENSP00000440508.2:p.Ser16Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.47C>T
  hgvsp: ENSP00000453983.1:p.Ser16Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-8C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.47C>T
  hgvsp: ENSP00000380264.3:p.Ser16Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.241G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-8C>T
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser16Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

14-24423045-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423045
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423045
    reference: chr 14
allele count: 1
allele frequency: 8.588999209812073e-6
allele num: 116428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.240C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.48G>A
  hgvsp: ENST00000397075.3:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.48G>A
  hgvsp: ENST00000559632.1:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.48G>A
  hgvsp: ENST00000397074.3:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.48G>A
  hgvsp: ENST00000313250.5:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.48G>A
  hgvsp: ENST00000543741.2:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-7G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.48G>A
  hgvsp: ENST00000558581.1:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.362C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12678C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.287C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-7G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.17C>T
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-7G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-7G>A
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.48G>A
  hgvsp: ENST00000558263.1:c.48G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser16Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

14-24423049-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423049
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423049
    reference: chr 14
allele count: 1
allele frequency: 8.674832575731289e-6
allele num: 115276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.52C>T
  hgvsp: ENSP00000380265.3:p.Arg18Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.358G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.52C>T
  hgvsp: ENSP00000452645.1:p.Arg18Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.13G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-3C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-3C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12682G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.52C>T
  hgvsp: ENSP00000380264.3:p.Arg18Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.52C>T
  hgvsp: ENSP00000440508.2:p.Arg18Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.52C>T
  hgvsp: ENSP00000453367.1:p.Arg18Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.236G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-3C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-3C>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.52C>T
  hgvsp: ENSP00000453983.1:p.Arg18Trp
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.283G>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.52C>T
  hgvsp: ENSP00000326219.5:p.Arg18Trp
  variant of: http://identifiers.org/hgnc/16985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24704
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg18Trp
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

14-24423050-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423050
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423050
    reference: chr 14
allele count: 3
allele frequency: 2.611329689077678e-5
allele num: 114884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.53G>T
  hgvsp: ENSP00000380265.3:p.Arg18Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.282C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.-2G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.-2G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.53G>T
  hgvsp: ENSP00000452645.1:p.Arg18Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.-2G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.-2G>T
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.235C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.53G>T
  hgvsp: ENSP00000380264.3:p.Arg18Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.357C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.53G>T
  hgvsp: ENSP00000326219.5:p.Arg18Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.53G>T
  hgvsp: ENSP00000440508.2:p.Arg18Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.53G>T
  hgvsp: ENSP00000453983.1:p.Arg18Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.53G>T
  hgvsp: ENSP00000453367.1:p.Arg18Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12683C>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.12C>A
  variant of: http://identifiers.org/hgnc/23175
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg18Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-24423052-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24423052
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 24423052
    reference: chr 14
allele count: 9
allele frequency: 7.890307195960162e-5
allele num: 114064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453367
  ensembl transcript: ENST00000558263
  gene symbol: DHRS4
  hgvsc: ENST00000558263.1:c.55A>T
  hgvsp: ENSP00000453367.1:p.Met19Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380263
  ensembl transcript: ENST00000397073
  gene symbol: DHRS4
  hgvsc: ENST00000397073.2:c.1A>T
  hgvsp: ENSP00000380263.2:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000556379
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000556379.1:n.355T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000558423
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000558423.1:n.112-12685T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000326219
  ensembl transcript: ENST00000313250
  gene symbol: DHRS4
  hgvsc: ENST00000313250.5:c.55A>T
  hgvsp: ENSP00000326219.5:p.Met19Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380264
  ensembl transcript: ENST00000397074
  gene symbol: DHRS4
  hgvsc: ENST00000397074.3:c.55A>T
  hgvsp: ENSP00000380264.3:p.Met19Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000404147
  ensembl transcript: ENST00000421831
  gene symbol: DHRS4
  hgvsc: ENST00000421831.1:c.1A>T
  hgvsp: ENSP00000404147.1:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000311993
  ensembl transcript: ENST00000308178
  gene symbol: DHRS4
  hgvsc: ENST00000308178.8:c.1A>T
  hgvsp: ENSP00000311993.8:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000553454
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000553454.1:n.280T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000372209
  ensembl transcript: ENST00000382761
  gene symbol: DHRS4
  hgvsc: ENST00000382761.3:c.1A>T
  hgvsp: ENSP00000372209.3:p.Met1?
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000380265
  ensembl transcript: ENST00000397075
  gene symbol: DHRS4
  hgvsc: ENST00000397075.3:c.55A>T
  hgvsp: ENSP00000380265.3:p.Met19Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000440508
  ensembl transcript: ENST00000543741
  gene symbol: DHRS4
  hgvsc: ENST00000543741.2:c.55A>T
  hgvsp: ENSP00000440508.2:p.Met19Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000554036
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000554036.1:n.10T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000452645
  ensembl transcript: ENST00000558581
  gene symbol: DHRS4
  hgvsc: ENST00000558581.1:c.55A>T
  hgvsp: ENSP00000452645.1:p.Met19Leu
  variant of: http://identifiers.org/hgnc/16985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000215256
  ensembl transcript: ENST00000555045
  gene symbol: DHRS4-AS1
  hgvsc: ENST00000555045.1:n.233T>A
  variant of: http://identifiers.org/hgnc/23175
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157326
  ensembl protein: ENSP00000453983
  ensembl transcript: ENST00000559632
  gene symbol: DHRS4
  hgvsc: ENST00000559632.1:c.55A>T
  hgvsp: ENSP00000453983.1:p.Met19Leu
  variant of: http://identifiers.org/hgnc/16985
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23672
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 43338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1319
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.759906304899473e-5
allele num: 10246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66250
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: 16510
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

FS
type: SiteQuality
SIO_000300: 1.127e0

QD
type: SiteQuality
SIO_000300: 2.057e1

DP
type: SiteQuality
SIO_000300: 3.374792e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.962e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.326e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.21e0

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

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

GenotypeQuality
all individuals: 8205
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42351
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1389
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510026576467746e-5
allele num: 66224
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.263e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.297e1

FS
type: SiteQuality
SIO_000300: 1.973e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.238e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.78e-1

DP
type: SiteQuality
SIO_000300: 3.291211e6

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-2

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

GenotypeQuality
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42352
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1628
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2320
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.687e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.623e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.438e0

DP
type: SiteQuality
SIO_000300: 3.285956e6

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.252e-1

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42346
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513134003147319e-5
allele num: 66088
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.7e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 2.6e-2

FS
type: SiteQuality
SIO_000300: 5.833e0

QD
type: SiteQuality
SIO_000300: 9.279999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.822e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 3.284132e6

GenotypeQuality
all individuals: 1456
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42347
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.636804461146806e-4
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.193e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

FS
type: SiteQuality
SIO_000300: 4.125e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

QD
type: SiteQuality
SIO_000300: 1.287e1

DP
type: SiteQuality
SIO_000300: 3.278029e6

GenotypeQuality
all individuals: 1575
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42345
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517957436473481e-5
allele num: 65878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.379e0

MQ
type: SiteQuality
SIO_000300: 5.918e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.58e-1

QD
type: SiteQuality
SIO_000300: 1.554e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.069e0

DP
type: SiteQuality
SIO_000300: 3.273589e6

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42346
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 955
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520450053215752e-5
allele num: 65770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 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: 9848
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

QD
type: SiteQuality
SIO_000300: 1.369e1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.37e0

FS
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 3.268459e6

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 897
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7196
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.015434606011373e-4
allele num: 9848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65770
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.213739531496541e-4
allele num: 16478
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.37e0

DP
type: SiteQuality
SIO_000300: 3.268459e6

QD
type: SiteQuality
SIO_000300: 1.369e1

FS
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

GenotypeQuality
all individuals: 159
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5220700152207e-5
allele num: 65700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.118e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: -3.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

DP
type: SiteQuality
SIO_000300: 3.265947e6

FS
type: SiteQuality
SIO_000300: 5.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

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

GenotypeQuality
all individuals: 1343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42340
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 893
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 7.001166861143524e-4
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

DP
type: SiteQuality
SIO_000300: 3.265947e6

QD
type: SiteQuality
SIO_000300: 1.118e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42341
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1624
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6640
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.577497024626934e-5
allele num: 65538
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.665e0

QD
type: SiteQuality
SIO_000300: 9.67e0

FS
type: SiteQuality
SIO_000300: 1.1782e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 3.259076e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 940
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1355
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42341
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525832341542311e-5
allele num: 65538
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.98e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.665e0

FS
type: SiteQuality
SIO_000300: 1.1782e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

DP
type: SiteQuality
SIO_000300: 3.259076e6

MQRankSum
type: SiteQuality
SIO_000300: 4.49e-1

QD
type: SiteQuality
SIO_000300: 9.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

GenotypeQuality
all individuals: 357
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6510
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
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: 1
allele frequency: 1.041016031646887e-4
allele num: 9606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65400
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.314e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

VQSLOD
type: SiteQuality
SIO_000300: -5.552e-1

DP
type: SiteQuality
SIO_000300: 3.25439e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.9e-1

GenotypeQuality
all individuals: 406
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1620
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65190
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.086427267194157e-5
allele num: 16430
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.414e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

VQSLOD
type: SiteQuality
SIO_000300: -5.185999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.989e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 3.24761e6

QD
type: SiteQuality
SIO_000300: 1.152e1

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

GenotypeQuality
all individuals: 1938
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1618
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2026
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9404
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.071441734750292e-5
allele num: 65116
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-2

DP
type: SiteQuality
SIO_000300: 3.244065e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.56e-1

FS
type: SiteQuality
SIO_000300: 3.512e0

QD
type: SiteQuality
SIO_000300: 1.468e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.75e-1

GenotypeQuality
all individuals: 207
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.08695652173913e-4
allele num: 9200
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 6.61e0

MQRankSum
type: SiteQuality
SIO_000300: 4.18e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.349e0

DP
type: SiteQuality
SIO_000300: 3.22959e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 5.338e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.945e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

GenotypeQuality
all individuals: 1724
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42334
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1612
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4372
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1306
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.110975311659741e-5
allele num: 16364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64672
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9162
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
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: 6568
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.888e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.38e-1

DP
type: SiteQuality
SIO_000300: 3.228264e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.12e0

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

MQ
type: SiteQuality
SIO_000300: 6.077e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

GenotypeQuality
all individuals: 1607
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42332
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 398
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8942
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.110710175132983e-5
allele num: 64294
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

DP
type: SiteQuality
SIO_000300: 3.219052e6

QD
type: SiteQuality
SIO_000300: 1.618e1

FS
type: SiteQuality
SIO_000300: 5.538e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 354
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42332
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 279
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 4.25e1
variant carriers: 0

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

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554871412134217e-5
allele num: 64314
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: 5.99e-1

DP
type: SiteQuality
SIO_000300: 3.218582e6

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.149e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

GenotypeQuality
all individuals: 279
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 8.75e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554871412134217e-5
allele num: 64314
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.353e1

FS
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.149e0

DP
type: SiteQuality
SIO_000300: 3.218582e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

GenotypeQuality
all individuals: 884
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8942
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55550024888004e-5
allele num: 64288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16334
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.892e1

FS
type: SiteQuality
SIO_000300: 3.502e0

VQSLOD
type: SiteQuality
SIO_000300: -1.847e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

DP
type: SiteQuality
SIO_000300: 3.217802e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.604e0

QD
type: SiteQuality
SIO_000300: 1.172e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.76e-1

GenotypeQuality
all individuals: 3049
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 7.5e0
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GenotypeQuality
all individuals: 755
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.674207721791156e-5
allele num: 64182
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

FS
type: SiteQuality
SIO_000300: 4.296e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.218e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.994e0

DP
type: SiteQuality
SIO_000300: 3.214325e6

VQSLOD
type: SiteQuality
SIO_000300: 9.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-1

GenotypeQuality
all individuals: 413
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1271
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 976
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.843657817109145e-4
allele num: 16272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64086
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 3.125e0

MQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.123e0

QD
type: SiteQuality
SIO_000300: 1.523e1

DP
type: SiteQuality
SIO_000300: 3.213801e6

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.351351351351351e-4
allele num: 7400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.65e-2

DP
type: SiteQuality
SIO_000300: 1.70546e5

QD
type: SiteQuality
SIO_000300: 1.181e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.274e0

VQSLOD
type: SiteQuality
SIO_000300: -1.11e0

MQ
type: SiteQuality
SIO_000300: 5.741e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 1.851362073525522e-3
allele num: 7562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.904e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

MQRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

QD
type: SiteQuality
SIO_000300: 1.264e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.42e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

DP
type: SiteQuality
SIO_000300: 1.80666e5

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3944
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.322401481089659e-4
allele num: 7562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.46e-1

FS
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 1.209e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

DP
type: SiteQuality
SIO_000300: 1.80061e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.250975292587776e-4
allele num: 3076
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.77e-2

DP
type: SiteQuality
SIO_000300: 1.66217e5

FS
type: SiteQuality
SIO_000300: 1.3222e1

MQRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.78e0

QD
type: SiteQuality
SIO_000300: 6.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2978
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.27e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.418e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.638e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 1.61198e5

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 1.015e1

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 5

African
type: Population
allele count: 111
allele frequency: 4.703389830508475e-1
allele num: 236
num of homozygotes: 25

European (Finnish)
type: Population
allele count: 14
allele frequency: 1.102362204724409e-2
allele num: 1270
num of homozygotes: 0

South Asian
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allele count: 451
allele frequency: 6.141067538126362e-2
allele num: 7344
num of homozygotes: 22

East Asian
type: Population
allele count: 1
allele frequency: 7.575757575757576e-3
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 6.122448979591837e-2
allele num: 98
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 4.320987654320987e-2
allele num: 162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 131
allele frequency: 4.492455418381344e-2
allele num: 2916
num of homozygotes: 3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.512e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.016e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

DP
type: SiteQuality
SIO_000300: 1.65095e5

QD
type: SiteQuality
SIO_000300: 1.457e1

FS
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.86e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 3

Other
type: Population
allele count: 4
allele frequency: 2.631578947368421e-2
allele num: 152
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 9.900990099009901e-3
allele num: 202
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.102040816326531e-2
allele num: 98
num of homozygotes: 0

South Asian
type: Population
allele count: 231
allele frequency: 3.283115406480955e-2
allele num: 7036
num of homozygotes: 9

East Asian
type: Population
allele count: 6
allele frequency: 4.545454545454546e-2
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 69
allele frequency: 2.480230050323508e-2
allele num: 2782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 19
allele frequency: 1.696428571428571e-2
allele num: 1120
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 1.261e0

QD
type: SiteQuality
SIO_000300: 1.596e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.93e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.5187e5

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.701242571582928e-4
allele num: 3702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1462
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.148e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.39e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

DP
type: SiteQuality
SIO_000300: 6.7975e4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.447e0

VQSLOD
type: SiteQuality
SIO_000300: -4.581e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.644e1

GenotypeQuality
all individuals: 190
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.759381898454746e-4
allele num: 3624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.35e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.228e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

QD
type: SiteQuality
SIO_000300: 4.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.78e-1

DP
type: SiteQuality
SIO_000300: 6.6075e4

MQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

MQ
type: SiteQuality
SIO_000300: 5.025e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.97e-1

GenotypeQuality
all individuals: 26
bin: 6.75e1
variant carriers: 25

Latino
type: Population
allele count: 2
allele frequency: 7.692307692307693e-2
allele num: 26
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 92
allele frequency: 1.446540880503145e-1
allele num: 636
num of homozygotes: 4

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.352941176470588e-2
allele num: 68
num of homozygotes: 1

Other
type: Population
allele count: 5
allele frequency: 1.388888888888889e-1
allele num: 36
num of homozygotes: 0

African
type: Population
allele count: 37
allele frequency: 6.166666666666667e-1
allele num: 60
num of homozygotes: 12

South Asian
type: Population
allele count: 242
allele frequency: 1.563307493540052e-1
allele num: 1548
num of homozygotes: 14

East Asian
type: Population
allele count: 8
allele frequency: 1.333333333333333e-1
allele num: 60
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.754e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.110000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.664e1

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

MQ
type: SiteQuality
SIO_000300: 4.71e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.6142e4

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8971
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 2570
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5783
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66128
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.394e0

FS
type: SiteQuality
SIO_000300: 1.585e0

QD
type: SiteQuality
SIO_000300: 9.050000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e0

DP
type: SiteQuality
SIO_000300: 1.776757e6

MQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.461e0

MQ
type: SiteQuality
SIO_000300: 5.734e1

GenotypeQuality
all individuals: 419
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
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variant carriers: 0

GenotypeQuality
all individuals: 490
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variant carriers: 0

GenotypeQuality
all individuals: 2548
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5778
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8958
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66102
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.966955153422502e-4
allele num: 10168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

FS
type: SiteQuality
SIO_000300: 1.973e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

DP
type: SiteQuality
SIO_000300: 1.77854e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 800
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variant carriers: 0

GenotypeQuality
all individuals: 697
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variant carriers: 0

GenotypeQuality
all individuals: 33771
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5778
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 2548
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.169031462060457e-5
allele num: 16210
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.484320557491289e-4
allele num: 8610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.210250824483374e-4
allele num: 66102
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 1.973e0

MQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

DP
type: SiteQuality
SIO_000300: 1.77854e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

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

GenotypeQuality
all individuals: 375
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5780
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 2550
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1305
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.734003814808393e-4
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 1.795478e6

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.066e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.26e-1

QD
type: SiteQuality
SIO_000300: 1.05e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 499
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variant carriers: 0

GenotypeQuality
all individuals: 36481
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 721
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variant carriers: 0

GenotypeQuality
all individuals: 162
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GenotypeQuality
all individuals: 5786
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 2640
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variant carriers: 0

GenotypeQuality
all individuals: 9201
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.322880371660859e-4
allele num: 8610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66290
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: -2.006e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.691e0

QD
type: SiteQuality
SIO_000300: 7.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

DP
type: SiteQuality
SIO_000300: 1.804143e6

GenotypeDepth
all individuals: 117
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variant carriers: 1

GenotypeDepth
all individuals: 235
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 723
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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
all individuals: 143
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GenotypeQuality
all individuals: 473
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 152
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GenotypeQuality
all individuals: 582
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507977199384745e-5
allele num: 66314
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.746588693957115e-5
allele num: 10260
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

DP
type: SiteQuality
SIO_000300: 1.805025e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 3.78e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

GenotypeDepth
all individuals: 433
bin: 6.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 9216
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 2645
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GenotypeQuality
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GenotypeQuality
all individuals: 145
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GenotypeQuality
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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: 36614
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 60
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 723
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 5787
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 2.094e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.991e1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.255e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-2

DP
type: SiteQuality
SIO_000300: 1.80549e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 147
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GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.597852441981296e-4
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66370
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.836e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

BaseQRankSum
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SIO_000300: -1.156e0

QD
type: SiteQuality
SIO_000300: 1.331e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e-1

DP
type: SiteQuality
SIO_000300: 1.808774e6

VQSLOD
type: SiteQuality
SIO_000300: -7.463e-1

GenotypeDepth
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variant carriers: 64

GenotypeDepth
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variant carriers: 58

GenotypeDepth
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variant carriers: 32

GenotypeQuality
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GenotypeQuality
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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: 978

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9199
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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: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 13
allele frequency: 1.125736058191895e-3
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 806
allele frequency: 1.214111409032025e-2
allele num: 66386
num of homozygotes: 4

African
type: Population
allele count: 14
allele frequency: 1.361073303519347e-3
allele num: 10286
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 7.777777777777778e-3
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 140
allele frequency: 2.140018343014369e-2
allele num: 6542
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-2

MQ
type: SiteQuality
SIO_000300: 5.949e1

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.49e0

QD
type: SiteQuality
SIO_000300: 1.277e1

DP
type: SiteQuality
SIO_000300: 1.824933e6

GenotypeDepth
all individuals: 12728
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variant carriers: 0

GenotypeDepth
all individuals: 280
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5150
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variant carriers: 6

GenotypeQuality
all individuals: 65
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 6.968641114982578e-4
allele num: 8610
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: 6536
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.79016e6

QD
type: SiteQuality
SIO_000300: 1.128e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 4.979e0

MQRankSum
type: SiteQuality
SIO_000300: -7.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

GenotypeDepth
all individuals: 339
bin: 7.75e1
variant carriers: 285

GenotypeDepth
all individuals: 566
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variant carriers: 480

GenotypeDepth
all individuals: 146
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variant carriers: 121

GenotypeDepth
all individuals: 1480
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variant carriers: 1003

GenotypeDepth
all individuals: 798
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variant carriers: 703

GenotypeQuality
all individuals: 96
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variant carriers: 18

GenotypeQuality
all individuals: 322
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variant carriers: 9

GenotypeQuality
all individuals: 2073
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variant carriers: 87

GenotypeQuality
all individuals: 2237
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variant carriers: 54

GenotypeQuality
all individuals: 16
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variant carriers: 9

GenotypeQuality
all individuals: 92
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variant carriers: 53

GenotypeQuality
all individuals: 16
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variant carriers: 9

GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 33
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variant carriers: 19

GenotypeQuality
all individuals: 16
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variant carriers: 11

GenotypeQuality
all individuals: 62
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variant carriers: 23

GenotypeQuality
all individuals: 826
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variant carriers: 85

GenotypeQuality
all individuals: 72
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variant carriers: 41

GenotypeQuality
all individuals: 72
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variant carriers: 41

GenotypeQuality
all individuals: 8669
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variant carriers: 67

GenotypeQuality
all individuals: 72
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variant carriers: 16

GenotypeQuality
all individuals: 353
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variant carriers: 98

GenotypeQuality
all individuals: 294
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variant carriers: 63

GenotypeQuality
all individuals: 35981
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variant carriers: 78

GenotypeQuality
all individuals: 9384
bin: 9.75e1
variant carriers: 8151

South Asian
type: Population
allele count: 944
allele frequency: 5.728850588663673e-2
allele num: 16478
num of homozygotes: 31

Other
type: Population
allele count: 59
allele frequency: 6.555555555555556e-2
allele num: 900
num of homozygotes: 3

Latino
type: Population
allele count: 644
allele frequency: 5.579622249176919e-2
allele num: 11542
num of homozygotes: 11

African
type: Population
allele count: 5693
allele frequency: 5.525038819875776e-1
allele num: 10304
num of homozygotes: 1580

European (Non-Finnish)
type: Population
allele count: 3154
allele frequency: 4.748140788245567e-2
allele num: 66426
num of homozygotes: 72

East Asian
type: Population
allele count: 42
allele frequency: 4.878048780487805e-3
allele num: 8610
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 53
allele frequency: 8.108935128518973e-3
allele num: 6536
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.919382e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.396e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

MQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

FS
type: SiteQuality
SIO_000300: 2.564e0

QD
type: SiteQuality
SIO_000300: 1.311e1

MQ
type: SiteQuality
SIO_000300: 5.74e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

GenotypeDepth
all individuals: 289
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1540
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variant carriers: 0

GenotypeDepth
all individuals: 215
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GenotypeDepth
all individuals: 26540
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variant carriers: 0

GenotypeDepth
all individuals: 2980
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7253
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GenotypeQuality
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GenotypeQuality
all individuals: 8929
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GenotypeQuality
all individuals: 2362
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GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 36343
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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
all individuals: 129
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1185
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GenotypeQuality
all individuals: 487
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66446
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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MQ
type: SiteQuality
SIO_000300: 5.99e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 2.975e1

BaseQRankSum
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SIO_000300: -2.146e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

DP
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SIO_000300: 1.893873e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

VQSLOD
type: SiteQuality
SIO_000300: 3.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2977
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variant carriers: 0

GenotypeDepth
all individuals: 1536
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variant carriers: 0

GenotypeDepth
all individuals: 4
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GenotypeDepth
all individuals: 389
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GenotypeDepth
all individuals: 289
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 270
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 72
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1184
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GenotypeQuality
all individuals: 2
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504936190705514e-5
allele num: 66448
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.893862e6

MQ
type: SiteQuality
SIO_000300: 5.871e1

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e-1

FS
type: SiteQuality
SIO_000300: 9.52e-1

GenotypeDepth
all individuals: 12236
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variant carriers: 0

GenotypeDepth
all individuals: 117
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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variant carriers: 7

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 6
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
all individuals: 70
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 47

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
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.073200096315916e-4
allele num: 66448
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: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 1.893812e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.061e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeDepth
all individuals: 267
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 323
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variant carriers: 0

GenotypeDepth
all individuals: 932
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 420
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.75e1
variant carriers: 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: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66432
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 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: 10356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

DP
type: SiteQuality
SIO_000300: 1.891979e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.966e0

QD
type: SiteQuality
SIO_000300: 1.179e1

VQSLOD
type: SiteQuality
SIO_000300: -2.058e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.141e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.25e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.703e1

GenotypeDepth
all individuals: 334
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 932
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 299
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
all individuals: 268
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variant carriers: 0

GenotypeDepth
all individuals: 605
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
all individuals: 420
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variant carriers: 0

GenotypeDepth
all individuals: 214
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variant carriers: 0

GenotypeDepth
all individuals: 269
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variant carriers: 1

GenotypeQuality
all individuals: 1
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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
all individuals: 8915
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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
all individuals: 486
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variant carriers: 0

GenotypeQuality
all individuals: 6
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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: 10

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 10
allele frequency: 1.160900859066636e-3
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
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: 66432
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.753e1

MQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

FS
type: SiteQuality
SIO_000300: 2.63e0

DP
type: SiteQuality
SIO_000300: 1.891904e6

VQSLOD
type: SiteQuality
SIO_000300: -5.133e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.3e-2

QD
type: SiteQuality
SIO_000300: 1.187e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

GenotypeDepth
all individuals: 275
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12252
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 765
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variant carriers: 0

GenotypeDepth
all individuals: 2971
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variant carriers: 0

GenotypeDepth
all individuals: 1530
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 420
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variant carriers: 0

GenotypeDepth
all individuals: 386
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variant carriers: 0

GenotypeDepth
all individuals: 268
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variant carriers: 0

GenotypeDepth
all individuals: 931
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variant carriers: 0

GenotypeDepth
all individuals: 162
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variant carriers: 0

GenotypeDepth
all individuals: 213
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GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
all individuals: 2362
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 7210
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variant carriers: 1

GenotypeQuality
all individuals: 126
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 432
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 2356
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GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 117
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 36164
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GenotypeQuality
all individuals: 164
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GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 717
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variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8908
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variant carriers: 0

GenotypeQuality
all individuals: 487
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505751972535084e-5
allele num: 66412
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.372e0

MQRankSum
type: SiteQuality
SIO_000300: -3.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.49e-1

MQ
type: SiteQuality
SIO_000300: 5.935e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

DP
type: SiteQuality
SIO_000300: 1.891552e6

FS
type: SiteQuality
SIO_000300: 1.1354e1

QD
type: SiteQuality
SIO_000300: 9.25e0

GenotypeDepth
all individuals: 12195
bin: 3.25e1
variant carriers: 834

GenotypeDepth
all individuals: 164
bin: 8.75e1
variant carriers: 142

GenotypeDepth
all individuals: 302
bin: 1.75e1
variant carriers: 195

GenotypeDepth
all individuals: 944
bin: 5.25e1
variant carriers: 800

GenotypeDepth
all individuals: 123
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variant carriers: 99

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 346
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variant carriers: 62

GenotypeDepth
all individuals: 797
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variant carriers: 705

GenotypeDepth
all individuals: 220
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variant carriers: 185

GenotypeDepth
all individuals: 473
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variant carriers: 429

GenotypeDepth
all individuals: 424
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variant carriers: 353

GenotypeDepth
all individuals: 2866
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variant carriers: 911

GenotypeQuality
all individuals: 13
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variant carriers: 10

GenotypeQuality
all individuals: 35895
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variant carriers: 78

GenotypeQuality
all individuals: 142
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variant carriers: 67

GenotypeQuality
all individuals: 21
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variant carriers: 7

GenotypeQuality
all individuals: 98
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variant carriers: 46

GenotypeQuality
all individuals: 22
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variant carriers: 14

GenotypeQuality
all individuals: 352
bin: 9.25e1
variant carriers: 99

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 14

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 41

GenotypeQuality
all individuals: 287
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variant carriers: 59

GenotypeQuality
all individuals: 8654
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variant carriers: 72

GenotypeQuality
all individuals: 43
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variant carriers: 25

GenotypeQuality
all individuals: 2229
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variant carriers: 52

GenotypeQuality
all individuals: 64
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variant carriers: 25

GenotypeQuality
all individuals: 439
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variant carriers: 16

GenotypeQuality
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variant carriers: 17

GenotypeQuality
all individuals: 9275
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variant carriers: 8087

GenotypeQuality
all individuals: 831
bin: 8.25e1
variant carriers: 94

GenotypeQuality
all individuals: 2057
bin: 7.75e1
variant carriers: 96

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 11

European (Non-Finnish)
type: Population
allele count: 3157
allele frequency: 4.754661284978463e-2
allele num: 66398
num of homozygotes: 73

Other
type: Population
allele count: 59
allele frequency: 6.555555555555556e-2
allele num: 900
num of homozygotes: 3

South Asian
type: Population
allele count: 945
allele frequency: 5.732136358122043e-2
allele num: 16486
num of homozygotes: 31

African
type: Population
allele count: 5657
allele frequency: 5.497570456754131e-1
allele num: 10290
num of homozygotes: 1562

Latino
type: Population
allele count: 644
allele frequency: 5.580589254766031e-2
allele num: 11540
num of homozygotes: 11

European (Finnish)
type: Population
allele count: 53
allele frequency: 8.146326467875806e-3
allele num: 6506
num of homozygotes: 0

East Asian
type: Population
allele count: 42
allele frequency: 4.876915931258709e-3
allele num: 8612
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.802e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.944e0

FS
type: SiteQuality
SIO_000300: 3.331e0

QD
type: SiteQuality
SIO_000300: 1.242e1

DP
type: SiteQuality
SIO_000300: 1.906185e6

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.369e-1

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

GenotypeDepth
all individuals: 29936
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variant carriers: 0

GenotypeDepth
all individuals: 587
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variant carriers: 0

GenotypeDepth
all individuals: 8
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GenotypeDepth
all individuals: 57
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GenotypeDepth
all individuals: 259
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GenotypeDepth
all individuals: 2250
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GenotypeDepth
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GenotypeDepth
all individuals: 207
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GenotypeDepth
all individuals: 55
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GenotypeDepth
all individuals: 645
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GenotypeDepth
all individuals: 237
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 152
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 81
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GenotypeQuality
all individuals: 138
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GenotypeQuality
all individuals: 783
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 40770
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GenotypeQuality
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GenotypeQuality
all individuals: 9680
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 141
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GenotypeQuality
all individuals: 327
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GenotypeQuality
all individuals: 2427
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GenotypeQuality
all individuals: 2493
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variant carriers: 2

GenotypeQuality
all individuals: 883
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507749834147518e-5
allele num: 66324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

FS
type: SiteQuality
SIO_000300: 1.905e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

DP
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SIO_000300: 1.737655e6

QD
type: SiteQuality
SIO_000300: 1.184e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.329e-1

MQ
type: SiteQuality
SIO_000300: 5.752e1

GenotypeDepth
all individuals: 259
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variant carriers: 3

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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.16144018583043e-3
allele num: 8610
num of homozygotes: 0

African
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allele frequency: 1.961938395134393e-4
allele num: 10194
num of homozygotes: 0

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66336
num of homozygotes: 0

East Asian
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allele num: 8610
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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FS
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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SIO_000300: -2.36e-1

VQSLOD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

South Asian
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allele count: 1
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num of homozygotes: 0

FS
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ReadPosRankSum
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ClippingRankSum
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QD
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MQ
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BaseQRankSum
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DP
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MQRankSum
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InbreedingCoeff
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SIO_000300: 2.0e-4

VQSLOD
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SIO_000300: -7.276e-1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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African
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allele count: 1
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allele num: 10062
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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VQSLOD
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 2

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66112
num of homozygotes: 0

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

Latino
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allele frequency: 1.567671137432503e-3
allele num: 11482
num of homozygotes: 0

East Asian
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Other
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South Asian
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African
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MQRankSum
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QD
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DP
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.518602885345482e-5
allele num: 65850
num of homozygotes: 0

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

DP
type: SiteQuality
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QD
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FS
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SIO_000300: 7.82e-1

MQRankSum
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SIO_000300: 9.350000000000001e-1

MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 25

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 3.039790862388668e-5
allele num: 65794
num of homozygotes: 0

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

Latino
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allele frequency: 3.50140056022409e-4
allele num: 11424
num of homozygotes: 0

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

African
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allele frequency: 1.665993537964459e-2
allele num: 9904
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East Asian
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

Other
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South Asian
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InbreedingCoeff
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QD
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
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SIO_000300: 5.781e1

BaseQRankSum
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SIO_000300: 1.54e0

DP
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SIO_000300: 1.698783e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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African
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Latino
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Other
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European (Finnish)
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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FS
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DP
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ReadPosRankSum
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QD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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Other
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East Asian
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African
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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FS
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QD
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BaseQRankSum
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VQSLOD
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DP
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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East Asian
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South Asian
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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FS
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.539408866995074e-5
allele num: 64960
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 3.08870768470472e-4
allele num: 16188
num of homozygotes: 0

FS
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QD
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: -8.0e-4

MQ
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SIO_000300: 5.96e1

ReadPosRankSum
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SIO_000300: 4.24e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.03777501037775e-4
allele num: 9636
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

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

FS
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SIO_000300: 1.4974e1

ReadPosRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.630449e6

QD
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VQSLOD
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GenotypeDepth
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variant carriers: 1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11148
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 64334
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East Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 2.25e-1

FS
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SIO_000300: 2.0714e1

DP
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InbreedingCoeff
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SIO_000300: -1.0e-3

MQ
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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SIO_000300: -7.000000000000001e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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Latino
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele count: 0
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ClippingRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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FS
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QD
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ReadPosRankSum
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MQRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

East Asian
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African
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.727387330601954e-5
allele num: 63460
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European (Finnish)
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Other
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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