14-68159300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159300
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159300
    reference: chr 14
allele count: 1
allele frequency: 8.728136019271725e-6
allele num: 114572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.165A>G
  hgvsp: ENST00000553384.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.204A>G
  hgvsp: ENST00000428130.2:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.204A>G
  hgvsp: ENST00000381346.4:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+351A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.85A>G
  hgvsp: ENSP00000452108.1:p.Ile29Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.218A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+351A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2162A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.269A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.634A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12513
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3448
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile29Val
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-68159304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159304
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159304
    reference: chr 14
allele count: 5
allele frequency: 4.391666373888908e-5
allele num: 113852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2166G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.161G>A
  hgvsp: ENSP00000452079.1:p.Arg54Gln
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+347G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.81G>A
  hgvsp: ENST00000557331.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.200G>A
  hgvsp: ENSP00000370750.4:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+347G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.200G>A
  hgvsp: ENSP00000416395.2:p.Arg67Gln
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.630G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.265G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.214G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12513
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg67Gln
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

14-68159314-TCAGCCAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159314
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159307
    reference: chr 14
allele count: 2
allele frequency: 1.774874871321572e-5
allele num: 112684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-11_208-5delTTGGCTG
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.613_619delTTGGCTG
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-11_155-5delTTGGCTG
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-11_75-5delTTGGCTG
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.248_254delTTGGCTG
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-11_194-5delTTGGCTG
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-11_194-5delTTGGCTG
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12512
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50799
  bin: 9.75e1
  variant carriers: 2
hgvs: c.194-11_194-5delTTGGCTG
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: TCAGCCAA
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-68159315-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159315
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159315
    reference: chr 14
allele count: 1
allele frequency: 8.878944471081278e-6
allele num: 112626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.254G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-5G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.619G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-5G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-5G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2177G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+336G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-5G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-5G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+336G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12510
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
hgvs: c.194-5G>A
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/14-68159318-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159318
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159318
    reference: chr 14
allele count: 1
allele frequency: 8.902341315766046e-6
allele num: 112330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.251G>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.616G>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-8G>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2180G>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+333G>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-8G>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-8G>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-8G>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-8G>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+333G>T
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50797
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: c.194-8G>T
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/14-68159320-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159320
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159320
    reference: chr 14
allele count: 1
allele frequency: 8.920924921495861e-6
allele num: 112096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.614T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-10T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+331T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-10T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-10T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-10T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+331T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.249T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-10T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2182T>G
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12509
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1538
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

14-68159327-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159327
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159327
    reference: chr 14
allele count: 1
allele frequency: 8.948706017109926e-6
allele num: 111748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.607C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+324C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-17C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+324C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-17C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-17C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-17C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.242C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-17C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2189C>A
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12510
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

14-68159331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159331
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159331
    reference: chr 14
allele count: 21
allele frequency: 1.8821926648263e-4
allele num: 111572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-21C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-21C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.603C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+320C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2193C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.238C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-21C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-21C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+320C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-21C>T
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12516
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

14-68159331-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159331
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159331
    reference: chr 14
allele count: 1
allele frequency: 8.962822213458574e-6
allele num: 111572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+320C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-21C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-21C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-21C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.603C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.238C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-21C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-21C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2193C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+320C>G
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12516
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

14-68159337-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159337
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159337
    reference: chr 14
allele count: 1
allele frequency: 8.991835413444593e-6
allele num: 111212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.232A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2199A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+314A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-27A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.597A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-27A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+314A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-27A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-27A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-27A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2867
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-68159339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159339
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159339
    reference: chr 14
allele count: 1
allele frequency: 8.994585259673677e-6
allele num: 111178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.595C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.230C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-29C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+312C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-29C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-29C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-29C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+312C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-29C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2201C>T
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

14-68159344-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159344
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159344
    reference: chr 14
allele count: 1
allele frequency: 9.006737039305401e-6
allele num: 111028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.225G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+307G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2206G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.590G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+307G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-34G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

14-68159354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159354
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159354
    reference: chr 14
allele count: 1
allele frequency: 9.023153411654306e-6
allele num: 110826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553578
  gene symbol: RDH11
  hgvsc: ENST00000553578.1:n.215C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+297C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.194-44C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.155-44C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2216C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.208-44C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.580C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+297C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-44C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.194-44C>T
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4569
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12499
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/14-68159602-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159602
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159602
    reference: chr 14
allele count: 3
allele frequency: 2.555322737261716e-5
allele num: 117402
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.193+49T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-292T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+49T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.193+49T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+49T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.332T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2464T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+88T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.207+49T>G
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3597
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5552
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-68159605-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159605
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159605
    reference: chr 14
allele count: 2
allele frequency: 1.702823280999898e-5
allele num: 117452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+46C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.207+46C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.329C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2467C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.193+46C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+85C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+46C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-295C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.193+46C>T
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7637
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2976
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5549
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

14-68159608-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159608
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159608
    reference: chr 14
allele count: 1
allele frequency: 8.510348583877996e-6
allele num: 117504
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.193+43T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.193+43T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2470T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.326T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+43T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.207+43T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+43T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-298T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+82T>C
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1550
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5563
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

14-68159615-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159615
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159615
    reference: chr 14
allele count: 2
allele frequency: 1.701172107582124e-5
allele num: 117566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2477G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.193+36G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.193+36G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+75G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.207+36G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-305G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+36G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.319G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+36G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10042
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5569
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11881
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2602
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-68159626-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159626
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159626
    reference: chr 14
allele count: 17421
allele frequency: 1.467797923968725e-1
allele num: 118688
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.193+25C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2488C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+25C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+25C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+64C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.193+25C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-316C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.308C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.207+25C>T
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.75e1
  variant carriers: 534
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 2.25e1
  variant carriers: 359
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 1.25e1
  variant carriers: 299
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 9.75e1
  variant carriers: 1891
genotype depth: GenotypeDepth
  all individuals: 9618
  bin: 3.25e1
  variant carriers: 375
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 8.25e1
  variant carriers: 605
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 7.25e1
  variant carriers: 1175
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 4.25e1
  variant carriers: 973
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 5.25e1
  variant carriers: 1429
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 6.25e1
  variant carriers: 1561
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.75e1
  variant carriers: 428
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 3.75e1
  variant carriers: 629
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 7.75e1
  variant carriers: 903
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 7.5e0
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 6.75e1
  variant carriers: 1415
genotype depth: GenotypeDepth
  all individuals: 10703
  bin: 2.75e1
  variant carriers: 306
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 4.75e1
  variant carriers: 1250
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 5.75e1
  variant carriers: 1579
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 387
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 2.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5357
  bin: 6.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 10
num of homozygotes: 1332
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS

14-68159628-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159628
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159628
    reference: chr 14
allele count: 1
allele frequency: 8.415808254224735e-6
allele num: 118824
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+23C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-318C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.306C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+23C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2490C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.193+23C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+62C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.207+23C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.193+23C>G
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8719
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14448
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4399
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

14-68159631-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159631
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159631
    reference: chr 14
allele count: 4
allele frequency: 3.362418251206268e-5
allele num: 118962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.193+20A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+20A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2493A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+20A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+59A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-321A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.303A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.207+20A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.193+20A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2257
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

14-68159632-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159632
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159632
    reference: chr 14
allele count: 1
allele frequency: 8.403785064793184e-6
allele num: 118994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.302A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2494A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-322A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.207+19A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+58A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.193+19A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.193+19A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.193+19A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.193+19A>T
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12760
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

14-68159656-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159656
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159656
    reference: chr 14
allele count: 1
allele frequency: 8.295726041943191e-6
allele num: 120544
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.188A>G
  hgvsp: ENSP00000370750.4:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+34A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.188A>G
  hgvsp: ENSP00000450651.1:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.188A>G
  hgvsp: ENSP00000450435.1:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.202A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.278A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2518A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.188A>G
  hgvsp: ENSP00000416395.2:p.Gln63Arg
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-346A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7516
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3455
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln63Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

14-68159669-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159669
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159669
    reference: chr 14
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.175A>G
  hgvsp: ENSP00000450651.1:p.Lys59Glu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.175A>G
  hgvsp: ENSP00000450435.1:p.Lys59Glu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2531A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.175A>G
  hgvsp: ENSP00000416395.2:p.Lys59Glu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.265A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+21A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.189A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.175A>G
  hgvsp: ENSP00000370750.4:p.Lys59Glu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-359A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7579
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys59Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-68159673-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159673
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159673
    reference: chr 14
allele count: 2
allele frequency: 1.650737054094653e-5
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.171A>G
  hgvsp: ENST00000557273.1:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.171A>G
  hgvsp: ENST00000381346.4:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.185A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2535A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.171A>G
  hgvsp: ENST00000557726.1:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+17A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.171A>G
  hgvsp: ENST00000428130.2:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.261A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-363A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr57Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-68159681-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159681
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159681
    reference: chr 14
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.163A>T
  hgvsp: ENSP00000450651.1:p.Lys55Ter
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.163A>T
  hgvsp: ENSP00000416395.2:p.Lys55Ter
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.177A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.163A>T
  hgvsp: ENSP00000370750.4:p.Lys55Ter
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2543A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.163A>T
  hgvsp: ENSP00000450435.1:p.Lys55Ter
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.253A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+9A>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-371A>T
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5976
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys55Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-68159685-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159685
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159685
    reference: chr 14
allele count: 2
allele frequency: 1.64923970049807e-5
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+5C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.159C>T
  hgvsp: ENST00000557726.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.159C>T
  hgvsp: ENST00000381346.4:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.173C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.249C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.159C>T
  hgvsp: ENST00000557273.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2547C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.159C>T
  hgvsp: ENST00000428130.2:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-375C>T
  variant of: http://identifiers.org/hgnc/17964
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5969
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4914
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: c.154+5C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

14-68159687-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159687
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159687
    reference: chr 14
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.157A>G
  hgvsp: ENSP00000416395.2:p.Ile53Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.157A>G
  hgvsp: ENSP00000370750.4:p.Ile53Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.154+3A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.157A>G
  hgvsp: ENSP00000450435.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.157A>G
  hgvsp: ENSP00000450651.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.247A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.171A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-377A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2549A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12766
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4362
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile53Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-68159696-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159696
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159696
    reference: chr 14
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.162A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.148A>G
  hgvsp: ENSP00000450435.1:p.Asn50Asp
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2558A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.148A>G
  hgvsp: ENSP00000452079.1:p.Asn50Asp
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-386A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.148A>G
  hgvsp: ENSP00000370750.4:p.Asn50Asp
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.238A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.148A>G
  hgvsp: ENSP00000450651.1:p.Asn50Asp
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.148A>G
  hgvsp: ENSP00000416395.2:p.Asn50Asp
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3447
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3273
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn50Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/14-68159707-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159707
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159707
    reference: chr 14
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.137T>G
  hgvsp: ENSP00000416395.2:p.Val46Gly
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.137T>G
  hgvsp: ENSP00000370750.4:p.Val46Gly
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-397T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.137T>G
  hgvsp: ENSP00000450435.1:p.Val46Gly
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2569T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.137T>G
  hgvsp: ENSP00000452079.1:p.Val46Gly
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.137T>G
  hgvsp: ENSP00000450651.1:p.Val46Gly
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.151T>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.227T>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3446
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val46Gly
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

14-68159707-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159707
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159707
    reference: chr 14
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.137T>C
  hgvsp: ENSP00000416395.2:p.Val46Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.137T>C
  hgvsp: ENSP00000452079.1:p.Val46Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.137T>C
  hgvsp: ENSP00000450651.1:p.Val46Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.137T>C
  hgvsp: ENSP00000370750.4:p.Val46Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.137T>C
  hgvsp: ENSP00000450435.1:p.Val46Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.227T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-397T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2569T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.151T>C
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14388
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val46Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

14-68159711-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159711
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159711
    reference: chr 14
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.133G>A
  hgvsp: ENSP00000370750.4:p.Val45Met
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.133G>A
  hgvsp: ENSP00000450435.1:p.Val45Met
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.133G>A
  hgvsp: ENSP00000450651.1:p.Val45Met
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-401G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.147G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.133G>A
  hgvsp: ENSP00000452079.1:p.Val45Met
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2573G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.223G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.133G>A
  hgvsp: ENSP00000416395.2:p.Val45Met
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val45Met
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

14-68159714-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159714
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159714
    reference: chr 14
allele count: 2
allele frequency: 1.648641519388024e-5
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.130G>A
  hgvsp: ENSP00000450435.1:p.Val44Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-404G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.220G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.130G>A
  hgvsp: ENSP00000452079.1:p.Val44Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.130G>A
  hgvsp: ENSP00000450651.1:p.Val44Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.144G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.130G>A
  hgvsp: ENSP00000416395.2:p.Val44Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.130G>A
  hgvsp: ENSP00000370750.4:p.Val44Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2576G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val44Ile
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS

14-68159722-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159722
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159722
    reference: chr 14
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2584G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.122G>A
  hgvsp: ENSP00000416395.2:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.122G>A
  hgvsp: ENSP00000450435.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.212G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.136G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.122G>A
  hgvsp: ENSP00000450651.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.122G>A
  hgvsp: ENSP00000452079.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.122G>A
  hgvsp: ENSP00000370750.4:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-412G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8645
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3249
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly41Glu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

14-68159723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159723
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159723
    reference: chr 14
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2585G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.121G>A
  hgvsp: ENSP00000416395.2:p.Gly41Arg
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.121G>A
  hgvsp: ENSP00000450435.1:p.Gly41Arg
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.135G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-413G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.121G>A
  hgvsp: ENSP00000450651.1:p.Gly41Arg
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.121G>A
  hgvsp: ENSP00000370750.4:p.Gly41Arg
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.211G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.121G>A
  hgvsp: ENSP00000452079.1:p.Gly41Arg
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12669
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8643
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4853
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2226
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly41Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

14-68159738-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159738
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159738
    reference: chr 14
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.106A>G
  hgvsp: ENSP00000450651.1:p.Thr36Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.106A>G
  hgvsp: ENSP00000450435.1:p.Thr36Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.106A>G
  hgvsp: ENSP00000416395.2:p.Thr36Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.75-2600A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.106A>G
  hgvsp: ENSP00000452079.1:p.Thr36Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.106A>G
  hgvsp: ENSP00000370750.4:p.Thr36Ala
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.120A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-428A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.196A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr36Ala
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

14-68159748-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159748
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159748
    reference: chr 14
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.110G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.96G>A
  hgvsp: ENST00000557726.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+2599G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.96G>A
  hgvsp: ENST00000381346.4:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.96G>A
  hgvsp: ENST00000553384.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.186G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.96G>A
  hgvsp: ENST00000428130.2:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.96G>A
  hgvsp: ENST00000557273.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-438G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3437
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val32Val
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

14-68159760-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159760
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159760
    reference: chr 14
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.84G>A
  hgvsp: ENST00000553384.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.84G>A
  hgvsp: ENST00000557726.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.174G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.84G>A
  hgvsp: ENST00000381346.4:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+2587G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.84G>A
  hgvsp: ENST00000428130.2:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.84G>A
  hgvsp: ENST00000557273.1:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.98G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-450G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu28Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

14-68159779-GAGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159779
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159776
    reference: chr 14
allele count: 4
allele frequency: 3.336781340718742e-5
allele num: 119876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.75-13_75-11delTCT
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.75-13_75-11delTCT
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.75-13_75-11delTCT
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-472_75-470delTCT
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.75-13_75-11delTCT
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.75-13_75-11delTCT
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+2565_74+2567delTCT
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.165-13_165-11delTCT
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.89-13_89-11delTCT
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: GAGA
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

14-68159790-CTCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159790
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159787
    reference: chr 14
allele count: 1
allele frequency: 8.375770570892522e-6
allele num: 119392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.165-24_165-22delTGA
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-483_75-481delTGA
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+2554_74+2556delTGA
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.75-24_75-22delTGA
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.75-24_75-22delTGA
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.75-24_75-22delTGA
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.75-24_75-22delTGA
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.75-24_75-22delTGA
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.89-24_89-22delTGA
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8549
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14349
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: CTCA
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

14-68159791-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159791
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159791
    reference: chr 14
allele count: 1
allele frequency: 8.370862701109976e-6
allele num: 119462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.165-22A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.75-22A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.75-22A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.75-22A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-481A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+2556A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.89-22A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.75-22A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.75-22A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4258
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14349
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ

14-68159800-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159800
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159800
    reference: chr 14
allele count: 1
allele frequency: 8.400961069946402e-6
allele num: 119034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.89-31G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.75-31G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.75-31G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.165-31G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.75-31G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-490G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.75-31G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+2547G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.75-31G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6301
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum

14-68159803-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159803
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159803
    reference: chr 14
allele count: 1
allele frequency: 8.412551526878102e-6
allele num: 118870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.75-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.75-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.89-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-493G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.75-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.75-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+2544G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.165-34G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.75-34G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11422
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14336
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

14-68159813-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68159813
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68159813
    reference: chr 14
allele count: 1
allele frequency: 8.460093737838614e-6
allele num: 118202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.75-44A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.75-503A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.75-44A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.75-44A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+2534A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.165-44A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.75-44A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.75-44A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.89-44A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2332
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

14-68162299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162299
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162299
    reference: chr 14
allele count: 1
allele frequency: 8.462384700008463e-6
allele num: 118170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+48G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+48G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+48G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+48G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+48G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+48G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+48G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+48G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+48G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ

14-68162300-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162300
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162300
    reference: chr 14
allele count: 2
allele frequency: 1.691446355778827e-5
allele num: 118242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+47C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+47C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+47C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+47C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+47C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+47C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+47C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+47C>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+47C>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17190
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2645
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7480
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2642
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1621
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3288
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

14-68162304-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162304
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162304
    reference: chr 14
allele count: 16
allele frequency: 1.350324921934341e-4
allele num: 118490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+43G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+43G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+43G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+43G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+43G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+43G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+43G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+43G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+43G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20126
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18022
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31829
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

14-68162308-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162308
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162308
    reference: chr 14
allele count: 1
allele frequency: 8.415666604951778e-6
allele num: 118826
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+39T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+39T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+39T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+39T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+39T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+39T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+39T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+39T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+39T>C
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18848
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

14-68162309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162309
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162309
    reference: chr 14
allele count: 2
allele frequency: 1.683189981653229e-5
allele num: 118822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+38G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+38G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+38G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+38G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+38G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+38G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+38G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+38G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+38G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19056
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2214
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

14-68162321-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162321
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162321
    reference: chr 14
allele count: 2
allele frequency: 1.673640167364017e-5
allele num: 119500
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+26T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+26T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+26T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+26T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+26T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+26T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+26T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+26T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+26T>C
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7867
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

14-68162327-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162327
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162327
    reference: chr 14
allele count: 290
allele frequency: 2.419529776902668e-3
allele num: 119858
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+20C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+20C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+20C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+20C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+20C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+20C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+20C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+20C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+20C>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 3.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8248
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 20501
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 25081
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1516
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

14-68162331-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162331
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162331
    reference: chr 14
allele count: 8
allele frequency: 6.663779029087395e-5
allele num: 120052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+16T>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+16T>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+16T>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+16T>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+16T>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+16T>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+16T>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+16T>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+16T>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20807
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2526
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

14-68162338-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162338
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162338
    reference: chr 14
allele count: 1
allele frequency: 8.313657676831499e-6
allele num: 120284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+9A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+9A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+9A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+9A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+9A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+9A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+9A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+9A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+9A>C
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2188
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

14-68162342-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162342
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162342
    reference: chr 14
allele count: 1
allele frequency: 8.307441806370146e-6
allele num: 120374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+5G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+5G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+5G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+5G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+5G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+5G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+5G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+5G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+5G>C
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2526
  bin: 7.75e1
  variant carriers: 0
hgvs: c.74+5G>C
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

14-68162346-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162346
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162346
    reference: chr 14
allele count: 1
allele frequency: 8.302062232258493e-6
allele num: 120452
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.88+1G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.74+1G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.74+1G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.74+1G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.74+1G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.74+1G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.164+1G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.74+1G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.74+1G>C
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 2.25e1
  variant carriers: 0
hgvs: c.74+1G>C
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: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP

14-68162351-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162351
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162351
    reference: chr 14
allele count: 1
allele frequency: 8.296001327360212e-6
allele num: 120540
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.70A>C
  hgvsp: ENSP00000370750.4:p.Ile24Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.70A>C
  hgvsp: ENSP00000416395.2:p.Ile24Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.70A>C
  hgvsp: ENSP00000451280.1:p.Ile24Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.70A>C
  hgvsp: ENSP00000450651.1:p.Ile24Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.70A>C
  hgvsp: ENSP00000452108.1:p.Ile24Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.70A>C
  hgvsp: ENSP00000452079.1:p.Ile24Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.84A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.160A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.70A>C
  hgvsp: ENSP00000450435.1:p.Ile24Leu
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1523
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile24Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-68162352-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162352
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162352
    reference: chr 14
allele count: 2
allele frequency: 1.659172736473594e-5
allele num: 120542
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.69A>C
  hgvsp: ENSP00000450651.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.69A>C
  hgvsp: ENSP00000452079.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.83A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.69A>C
  hgvsp: ENSP00000416395.2:p.Gln23His
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.69A>C
  hgvsp: ENSP00000452108.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.69A>C
  hgvsp: ENSP00000450435.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.159A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.69A>C
  hgvsp: ENSP00000451280.1:p.Gln23His
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.69A>C
  hgvsp: ENSP00000370750.4:p.Gln23His
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln23His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

14-68162364-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162364
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162364
    reference: chr 14
allele count: 2
allele frequency: 1.657797450307521e-5
allele num: 120642
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.57G>C
  hgvsp: ENSP00000416395.2:p.Met19Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.57G>C
  hgvsp: ENSP00000450435.1:p.Met19Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.57G>C
  hgvsp: ENSP00000370750.4:p.Met19Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.71G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.57G>C
  hgvsp: ENSP00000452079.1:p.Met19Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.147G>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.57G>C
  hgvsp: ENSP00000452108.1:p.Met19Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.57G>C
  hgvsp: ENSP00000450651.1:p.Met19Ile
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.57G>C
  hgvsp: ENSP00000451280.1:p.Met19Ile
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Met19Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

14-68162366-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162366
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162366
    reference: chr 14
allele count: 3
allele frequency: 2.486531288852051e-5
allele num: 120650
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.69A>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.55A>G
  hgvsp: ENSP00000370750.4:p.Met19Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.55A>G
  hgvsp: ENSP00000450651.1:p.Met19Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.55A>G
  hgvsp: ENSP00000452079.1:p.Met19Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.55A>G
  hgvsp: ENSP00000452108.1:p.Met19Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.55A>G
  hgvsp: ENSP00000451280.1:p.Met19Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.55A>G
  hgvsp: ENSP00000450435.1:p.Met19Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.55A>G
  hgvsp: ENSP00000416395.2:p.Met19Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.145A>G
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41807
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Met19Val
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

14-68162371-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162371
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162371
    reference: chr 14
allele count: 2
allele frequency: 1.657989853102099e-5
allele num: 120628
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.50T>C
  hgvsp: ENSP00000452108.1:p.Leu17Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.50T>C
  hgvsp: ENSP00000450651.1:p.Leu17Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.50T>C
  hgvsp: ENSP00000452079.1:p.Leu17Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.64T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.140T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.50T>C
  hgvsp: ENSP00000416395.2:p.Leu17Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.50T>C
  hgvsp: ENSP00000451280.1:p.Leu17Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.50T>C
  hgvsp: ENSP00000450435.1:p.Leu17Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.50T>C
  hgvsp: ENSP00000370750.4:p.Leu17Pro
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu17Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

14-68162375-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162375
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162375
    reference: chr 14
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.46C>G
  hgvsp: ENSP00000370750.4:p.Leu16Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.46C>G
  hgvsp: ENSP00000416395.2:p.Leu16Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.136C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.60C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.46C>G
  hgvsp: ENSP00000452079.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.46C>G
  hgvsp: ENSP00000452108.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.46C>G
  hgvsp: ENSP00000450651.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.46C>G
  hgvsp: ENSP00000451280.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.46C>G
  hgvsp: ENSP00000450435.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu16Val
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

14-68162376-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162376
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162376
    reference: chr 14
allele count: 7
allele frequency: 5.803541818664191e-5
allele num: 120616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.59C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.45C>G
  hgvsp: ENSP00000450651.1:p.Phe15Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.135C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.45C>G
  hgvsp: ENSP00000451280.1:p.Phe15Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.45C>G
  hgvsp: ENSP00000416395.2:p.Phe15Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.45C>G
  hgvsp: ENSP00000452108.1:p.Phe15Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.45C>G
  hgvsp: ENSP00000452079.1:p.Phe15Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.45C>G
  hgvsp: ENSP00000450435.1:p.Phe15Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.45C>G
  hgvsp: ENSP00000370750.4:p.Phe15Leu
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8426
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25244
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe15Leu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-68162379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162379
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162379
    reference: chr 14
allele count: 1
allele frequency: 8.290499088045101e-6
allele num: 120620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.42C>T
  hgvsp: ENST00000428130.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.132C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.42C>T
  hgvsp: ENST00000554731.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.42C>T
  hgvsp: ENST00000557331.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.42C>T
  hgvsp: ENST00000557273.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.42C>T
  hgvsp: ENST00000381346.4:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.56C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.42C>T
  hgvsp: ENST00000553384.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.42C>T
  hgvsp: ENST00000557726.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21539
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro14Pro
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

14-68162387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162387
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162387
    reference: chr 14
allele count: 1
allele frequency: 8.295175525914129e-6
allele num: 120552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.34C>T
  hgvsp: ENSP00000416395.2:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.34C>T
  hgvsp: ENSP00000451280.1:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.34C>T
  hgvsp: ENSP00000450651.1:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.34C>T
  hgvsp: ENSP00000370750.4:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.34C>T
  hgvsp: ENSP00000452108.1:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.34C>T
  hgvsp: ENSP00000450435.1:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.34C>T
  hgvsp: ENSP00000452079.1:p.Leu12Phe
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.48C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.124C>T
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu12Phe
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

14-68162389-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162389
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162389
    reference: chr 14
allele count: 1
allele frequency: 8.295863682367972e-6
allele num: 120542
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.32T>C
  hgvsp: ENSP00000452108.1:p.Leu11Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.32T>C
  hgvsp: ENSP00000416395.2:p.Leu11Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.32T>C
  hgvsp: ENSP00000452079.1:p.Leu11Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.46T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.32T>C
  hgvsp: ENSP00000370750.4:p.Leu11Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.32T>C
  hgvsp: ENSP00000450435.1:p.Leu11Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.32T>C
  hgvsp: ENSP00000450651.1:p.Leu11Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.32T>C
  hgvsp: ENSP00000451280.1:p.Leu11Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.122T>C
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8144
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2503
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu11Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

14-68162391-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162391
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162391
    reference: chr 14
allele count: 1
allele frequency: 8.297515723792297e-6
allele num: 120518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.120C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.44C>T
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.30C>T
  hgvsp: ENST00000381346.4:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.30C>T
  hgvsp: ENST00000557331.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.30C>T
  hgvsp: ENST00000428130.2:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.30C>T
  hgvsp: ENST00000553384.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.30C>T
  hgvsp: ENST00000554731.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.30C>T
  hgvsp: ENST00000557273.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.30C>T
  hgvsp: ENST00000557726.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8136
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu10Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

14-68162393-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162393
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162393
    reference: chr 14
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.118C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.28C>G
  hgvsp: ENSP00000452079.1:p.Leu10Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.28C>G
  hgvsp: ENSP00000452108.1:p.Leu10Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.28C>G
  hgvsp: ENSP00000450435.1:p.Leu10Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.42C>G
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.28C>G
  hgvsp: ENSP00000450651.1:p.Leu10Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.28C>G
  hgvsp: ENSP00000451280.1:p.Leu10Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.28C>G
  hgvsp: ENSP00000370750.4:p.Leu10Val
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.28C>G
  hgvsp: ENSP00000416395.2:p.Leu10Val
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8414
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu10Val
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

14-68162394-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162394
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162394
    reference: chr 14
allele count: 1
allele frequency: 8.299168423323983e-6
allele num: 120494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.117G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.27G>A
  hgvsp: ENST00000554731.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.27G>A
  hgvsp: ENST00000553384.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.27G>A
  hgvsp: ENST00000428130.2:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.27G>A
  hgvsp: ENST00000381346.4:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.27G>A
  hgvsp: ENST00000557331.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.27G>A
  hgvsp: ENST00000557726.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.41G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.27G>A
  hgvsp: ENST00000557273.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41663
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu9Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

14-68162397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162397
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162397
    reference: chr 14
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.24G>A
  hgvsp: ENST00000381346.4:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.24G>A
  hgvsp: ENST00000557273.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.24G>A
  hgvsp: ENST00000554731.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.24G>A
  hgvsp: ENST00000557726.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.24G>A
  hgvsp: ENST00000553384.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.38G>A
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.24G>A
  hgvsp: ENST00000428130.2:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.24G>A
  hgvsp: ENST00000557331.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.114G>A
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu8Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

14-68162398-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162398
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162398
    reference: chr 14
allele count: 18
allele frequency: 1.49442082890542e-4
allele num: 120448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.23T>C
  hgvsp: ENSP00000451280.1:p.Leu8Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.23T>C
  hgvsp: ENSP00000452079.1:p.Leu8Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.113T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.23T>C
  hgvsp: ENSP00000452108.1:p.Leu8Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.37T>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.23T>C
  hgvsp: ENSP00000450651.1:p.Leu8Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.23T>C
  hgvsp: ENSP00000450435.1:p.Leu8Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.23T>C
  hgvsp: ENSP00000370750.4:p.Leu8Pro
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.23T>C
  hgvsp: ENSP00000416395.2:p.Leu8Pro
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8122
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41584
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu8Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

14-68162408-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68162408
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 68162408
    reference: chr 14
allele count: 1
allele frequency: 8.313381218409152e-6
allele num: 120288
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000370750
  ensembl transcript: ENST00000381346
  gene symbol: RDH11
  hgvsc: ENST00000381346.4:c.13A>C
  hgvsp: ENSP00000370750.4:p.Met5Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000553816
  gene symbol: RDH11
  hgvsc: ENST00000553816.1:n.27A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452108
  ensembl transcript: ENST00000557331
  gene symbol: RDH11
  hgvsc: ENST00000557331.1:c.13A>C
  hgvsp: ENSP00000452108.1:p.Met5Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000451280
  ensembl transcript: ENST00000554731
  gene symbol: RDH11
  hgvsc: ENST00000554731.1:c.13A>C
  hgvsp: ENSP00000451280.1:p.Met5Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072042
  ensembl transcript: ENST00000556692
  gene symbol: RDH11
  hgvsc: ENST00000556692.1:n.103A>C
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450651
  ensembl transcript: ENST00000557273
  gene symbol: RDH11
  hgvsc: ENST00000557273.1:c.13A>C
  hgvsp: ENSP00000450651.1:p.Met5Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000450435
  ensembl transcript: ENST00000557726
  gene symbol: RDH11
  hgvsc: ENST00000557726.1:c.13A>C
  hgvsp: ENSP00000450435.1:p.Met5Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000416395
  ensembl transcript: ENST00000428130
  gene symbol: RDH11
  hgvsc: ENST00000428130.2:c.13A>C
  hgvsp: ENSP00000416395.2:p.Met5Leu
  variant of: http://identifiers.org/hgnc/17964
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072042
  ensembl protein: ENSP00000452079
  ensembl transcript: ENST00000553384
  gene symbol: RDH11
  hgvsc: ENST00000553384.1:c.13A>C
  hgvsp: ENSP00000452079.1:p.Met5Leu
  variant of: http://identifiers.org/hgnc/17964
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met5Leu
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 95
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50800
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 816
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1618
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 576
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11692
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163873370577281e-4
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65006
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.142e0

DP
type: SiteQuality
SIO_000300: 4.389792e6

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.23e0

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-2

QD
type: SiteQuality
SIO_000300: 1.498e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.66e-1

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

GenotypeQuality
all individuals: 50803
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1038
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 183
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 499
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11220
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.863813229571985e-4
allele num: 10280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64788
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 4.386978e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.465e0

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
all individuals: 1553
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2737
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.099333643266698e-5
allele num: 64530
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.303e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-2

DP
type: SiteQuality
SIO_000300: 4.378877e6

MQRankSum
type: SiteQuality
SIO_000300: -7.672e0

FS
type: SiteQuality
SIO_000300: 4.268e0

QD
type: SiteQuality
SIO_000300: 6.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

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

GenotypeQuality
all individuals: 94
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 50797
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1658
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 304
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549762886278399e-5
allele num: 64526
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.291e0

FS
type: SiteQuality
SIO_000300: 1.514e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.101e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

VQSLOD
type: SiteQuality
SIO_000300: 5.18e-1

DP
type: SiteQuality
SIO_000300: 4.378595e6

QD
type: SiteQuality
SIO_000300: 1.279e1

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 308
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1832
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1547
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.750390015600624e-5
allele num: 10256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64440
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

DP
type: SiteQuality
SIO_000300: 4.376473e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.45e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 258
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2421
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 6.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50796
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.070000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.429e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 2.194e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.929e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.25e0

DP
type: SiteQuality
SIO_000300: 4.374292e6

GenotypeQuality
all individuals: 2326
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 484
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50798
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2160
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554436361375365e-5
allele num: 64332
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

QD
type: SiteQuality
SIO_000300: 1.014e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.81e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

DP
type: SiteQuality
SIO_000300: 4.371453e6

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9578
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: 21
allele frequency: 3.266245683889632e-4
allele num: 64294
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.81e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.366e1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

FS
type: SiteQuality
SIO_000300: 9.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

DP
type: SiteQuality
SIO_000300: 4.369196e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555355087566491e-5
allele num: 64294
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.366e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

DP
type: SiteQuality
SIO_000300: 4.369196e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

FS
type: SiteQuality
SIO_000300: 9.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.81e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64200
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9340
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.363492e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

FS
type: SiteQuality
SIO_000300: 7.055e0

QD
type: SiteQuality
SIO_000300: 1.294e1

MQRankSum
type: SiteQuality
SIO_000300: -8.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 1.072731173567904e-4
allele num: 9322
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64192
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.362838e6

MQRankSum
type: SiteQuality
SIO_000300: -9.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.588e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.507e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

QD
type: SiteQuality
SIO_000300: 1.998e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559040878051823e-5
allele num: 64142
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.849e-1

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.360417e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.05e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.172332942555686e-4
allele num: 8530
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10170
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64100
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.355116e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.43e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 3
allele frequency: 3.472222222222222e-4
allele num: 8640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65702
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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QD
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.365e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.78e0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521560512461581e-5
allele num: 65722
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

FS
type: SiteQuality
SIO_000300: 1.263e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

QD
type: SiteQuality
SIO_000300: 8.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

DP
type: SiteQuality
SIO_000300: 2.414623e6

VQSLOD
type: SiteQuality
SIO_000300: -1.148e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23414
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 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: 13762
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52151421094273e-5
allele num: 65724
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.062e0

FS
type: SiteQuality
SIO_000300: 2.249e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

QD
type: SiteQuality
SIO_000300: 8.199999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.897e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 2.415691e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-2

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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1897
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variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.041917624870719e-5
allele num: 65748
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.42e-1

QD
type: SiteQuality
SIO_000300: 1.036e1

DP
type: SiteQuality
SIO_000300: 2.419247e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.24e-1

FS
type: SiteQuality
SIO_000300: 7.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.373e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1645
bin: 8.75e1
variant carriers: 35

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 4

GenotypeQuality
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variant carriers: 15

GenotypeQuality
all individuals: 48
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GenotypeQuality
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bin: 9.25e1
variant carriers: 33

GenotypeQuality
all individuals: 481
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variant carriers: 7

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 14

GenotypeQuality
all individuals: 2424
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variant carriers: 14

GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 37

GenotypeQuality
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variant carriers: 20

GenotypeQuality
all individuals: 26407
bin: 9.75e1
variant carriers: 15848

GenotypeQuality
all individuals: 3630
bin: 7.75e1
variant carriers: 33

GenotypeQuality
all individuals: 585
bin: 3.25e1
variant carriers: 14

European (Finnish)
type: Population
allele count: 1097
allele frequency: 1.659606656580938e-1
allele num: 6610
num of homozygotes: 101

European (Non-Finnish)
type: Population
allele count: 10002
allele frequency: 1.514766015447524e-1
allele num: 66030
num of homozygotes: 729

African
type: Population
allele count: 959
allele frequency: 9.247830279652845e-2
allele num: 10370
num of homozygotes: 53

Latino
type: Population
allele count: 1775
allele frequency: 1.535732825748399e-1
allele num: 11558
num of homozygotes: 149

East Asian
type: Population
allele count: 1769
allele frequency: 2.046032847559565e-1
allele num: 8646
num of homozygotes: 183

Other
type: Population
allele count: 133
allele frequency: 1.521739130434783e-1
allele num: 874
num of homozygotes: 8

South Asian
type: Population
allele count: 1686
allele frequency: 1.154794520547945e-1
allele num: 14600
num of homozygotes: 109

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.436e1

VQSLOD
type: SiteQuality
SIO_000300: 5.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.099e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

DP
type: SiteQuality
SIO_000300: 2.601889e6

FS
type: SiteQuality
SIO_000300: 5.45e-1

GenotypeQuality
all individuals: 3461
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
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GenotypeQuality
all individuals: 3327
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 251
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variant carriers: 0

GenotypeQuality
all individuals: 205
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GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 484
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GenotypeQuality
all individuals: 664
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variant carriers: 0

GenotypeQuality
all individuals: 2255
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variant carriers: 0

GenotypeQuality
all individuals: 16541
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7405
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variant carriers: 0

GenotypeQuality
all individuals: 4953
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14692
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66056
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.117094e6

MQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.319e0

FS
type: SiteQuality
SIO_000300: 9.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.32e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.578e-1

MQ
type: SiteQuality
SIO_000300: 5.894e1

QD
type: SiteQuality
SIO_000300: 1.449e1

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4957
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GenotypeQuality
all individuals: 1255
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GenotypeQuality
all individuals: 14446
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
all individuals: 7410
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4395
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14794
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-5
allele num: 66080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.593360995850622e-4
allele num: 11568
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.931e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-1

FS
type: SiteQuality
SIO_000300: 2.737e0

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

DP
type: SiteQuality
SIO_000300: 2.11978e6

MQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

QD
type: SiteQuality
SIO_000300: 1.053e1

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4392
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variant carriers: 0

GenotypeQuality
all individuals: 170
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variant carriers: 0

GenotypeQuality
all individuals: 234
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variant carriers: 0

GenotypeQuality
all individuals: 472
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GenotypeQuality
all individuals: 1237
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7408
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variant carriers: 0

GenotypeQuality
all individuals: 14444
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66086
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14818
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

FS
type: SiteQuality
SIO_000300: 5.195e0

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.222e0

VQSLOD
type: SiteQuality
SIO_000300: 4.43e-1

DP
type: SiteQuality
SIO_000300: 2.120562e6

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 54
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 14426
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 57
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GenotypeQuality
all individuals: 4
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15954
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.18e-1

DP
type: SiteQuality
SIO_000300: 2.147e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.044e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.081e0

FS
type: SiteQuality
SIO_000300: 8.43e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.479e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.08e-1

GenotypeQuality
all individuals: 19850
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 14417
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GenotypeQuality
all individuals: 4936
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 3451
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 2248
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variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

MQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

FS
type: SiteQuality
SIO_000300: 6.292e0

DP
type: SiteQuality
SIO_000300: 2.153904e6

VQSLOD
type: SiteQuality
SIO_000300: 7.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003003003003003e-5
allele num: 66600
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 6.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

DP
type: SiteQuality
SIO_000300: 2.154812e6

VQSLOD
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SIO_000300: 2.5e0

QD
type: SiteQuality
SIO_000300: 1.537e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.26e-1

FS
type: SiteQuality
SIO_000300: 7.013e0

DP
type: SiteQuality
SIO_000300: 2.155011e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.523e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.473e1

VQSLOD
type: SiteQuality
SIO_000300: -1.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.022e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.213592233009709e-4
allele num: 16480
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.307e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

FS
type: SiteQuality
SIO_000300: 3.012e0

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

DP
type: SiteQuality
SIO_000300: 2.154907e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
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: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.07e-1

DP
type: SiteQuality
SIO_000300: 2.154534e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.448e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

FS
type: SiteQuality
SIO_000300: 5.449e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-2

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e-1

FS
type: SiteQuality
SIO_000300: 3.97e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.479e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.595e1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.153646e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

South Asian
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allele frequency: 6.062810719049351e-5
allele num: 16494
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.654e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

South Asian
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allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

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

Other
type: Population
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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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num of homozygotes: 0

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

FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

South Asian
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allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: -2.531e0

ClippingRankSum
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QD
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ReadPosRankSum
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SIO_000300: 2.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

VQSLOD
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MQ
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DP
type: SiteQuality
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FS
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SIO_000300: 0.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.727e0

MQRankSum
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SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.849e0

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.19e1

DP
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SIO_000300: 2.152751e6

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

South Asian
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allele frequency: 1.212856276531231e-4
allele num: 16490
num of homozygotes: 0

MQRankSum
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SIO_000300: 1.14e0

BaseQRankSum
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SIO_000300: -7.05e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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FS
type: SiteQuality
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ReadPosRankSum
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DP
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ClippingRankSum
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SIO_000300: 5.4e-1

QD
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VQSLOD
type: SiteQuality
SIO_000300: 6.26e-1

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.182e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

Other
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.1e-1

ClippingRankSum
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QD
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MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.776e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.81e-1

DP
type: SiteQuality
SIO_000300: 2.14856e6

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

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

Other
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African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
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Latino
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BaseQRankSum
type: SiteQuality
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MQ
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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VQSLOD
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FS
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

South Asian
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.524613899613899e-5
allele num: 66304
num of homozygotes: 0

Other
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MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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DP
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FS
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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Latino
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African
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South Asian
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Other
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MQ
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 8.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15272
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510756586898719e-5
allele num: 66192
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

DP
type: SiteQuality
SIO_000300: 2.08083e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

QD
type: SiteQuality
SIO_000300: 1.215e1

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14998
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.375e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.152e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.274e0

MQ
type: SiteQuality
SIO_000300: 5.887e1

FS
type: SiteQuality
SIO_000300: 5.636e0

DP
type: SiteQuality
SIO_000300: 2.050744e6

QD
type: SiteQuality
SIO_000300: 1.16e1

MQRankSum
type: SiteQuality
SIO_000300: 4.51e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14900
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.045476e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.86e-1

BaseQRankSum
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SIO_000300: -1.837e0

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.418e-1

FS
type: SiteQuality
SIO_000300: 3.92e0

QD
type: SiteQuality
SIO_000300: 7.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.92e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518695137138171e-5
allele num: 65846
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14512
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

DP
type: SiteQuality
SIO_000300: 2.006341e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.17e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15678
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.875567845151097e-5
allele num: 10126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

MQRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -9.782e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.82e-1

DP
type: SiteQuality
SIO_000300: 1.493809e6

QD
type: SiteQuality
SIO_000300: 1.893e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.071158748195694e-5
allele num: 65122
num of homozygotes: 0

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

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-2

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 12
allele frequency: 1.183898973954223e-3
allele num: 10136
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.729050279329609e-5
allele num: 11456
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6484
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East Asian
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allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.266303659617576e-4
allele num: 15794
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.533272002453235e-5
allele num: 65220
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

BaseQRankSum
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DP
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SIO_000300: 1.525262e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65362
num of homozygotes: 0

European (Finnish)
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allele num: 6504
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African
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allele frequency: 9.832841691248771e-5
allele num: 10170
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 15906
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65374
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.343017806935333e-4
allele num: 8536
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.94e-1

QD
type: SiteQuality
SIO_000300: 1.178e1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.56e-1

FS
type: SiteQuality
SIO_000300: 3.751e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.626e0

DP
type: SiteQuality
SIO_000300: 1.554485e6

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

GenotypeQuality
all individuals: 276
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 645
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2212
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39361
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.045066991473813e-5
allele num: 65680
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: 11484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.692e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

DP
type: SiteQuality
SIO_000300: 1.590749e6

QD
type: SiteQuality
SIO_000300: 1.421e1

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2447
bin: 9.75e1
variant carriers: 288

GenotypeQuality
all individuals: 838
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40348
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7936
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 23
allele frequency: 2.001740644038294e-3
allele num: 11490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.557746650056213e-5
allele num: 65822
num of homozygotes: 0

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

African
type: Population
allele count: 264
allele frequency: 2.568593111500292e-2
allele num: 10278
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.607635e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

QD
type: SiteQuality
SIO_000300: 1.355e1

VQSLOD
type: SiteQuality
SIO_000300: 5.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.397e0

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

GenotypeQuality
all individuals: 40781
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
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variant carriers: 0

GenotypeQuality
all individuals: 8040
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variant carriers: 0

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

GenotypeQuality
all individuals: 1529
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2193
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 583
bin: 8.75e1
variant carriers: 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: 10306
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.297642436149312e-4
allele num: 16288
num of homozygotes: 1

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: 65898
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

DP
type: SiteQuality
SIO_000300: 1.608296e6

MQRankSum
type: SiteQuality
SIO_000300: 4.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.24e-2

QD
type: SiteQuality
SIO_000300: 1.296e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.088e0

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

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 583
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 2531
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variant carriers: 0

GenotypeQuality
all individuals: 203
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variant carriers: 0

GenotypeQuality
all individuals: 41119
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variant carriers: 0

GenotypeQuality
all individuals: 8098
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variant carriers: 0

GenotypeQuality
all individuals: 127
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variant carriers: 0

GenotypeQuality
all individuals: 776
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variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515748628247491e-5
allele num: 65974
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 10328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.62e0

QD
type: SiteQuality
SIO_000300: 1.384e1

VQSLOD
type: SiteQuality
SIO_000300: 9.15e-1

FS
type: SiteQuality
SIO_000300: 4.297e0

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

DP
type: SiteQuality
SIO_000300: 1.613792e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

GenotypeQuality
all individuals: 1522
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 2188
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41361
bin: 6.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66014
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
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: 16402
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

QD
type: SiteQuality
SIO_000300: 7.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.211e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.616737e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.684e-1

GenotypeQuality
all individuals: 8116
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41513
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 776
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2188
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514096235956757e-5
allele num: 66046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.186e0

MQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.477e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

DP
type: SiteQuality
SIO_000300: 1.618412e6

GenotypeQuality
all individuals: 776
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2185
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 583
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
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GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2325
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2531
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66090
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.683e0

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

DP
type: SiteQuality
SIO_000300: 1.620038e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.114e1

FS
type: SiteQuality
SIO_000300: 7.54e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.61e-1

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 584
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2187
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 491
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 777
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variant carriers: 0

GenotypeQuality
all individuals: 8135
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41652
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51308821304282e-5
allele num: 66090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
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: 8634
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

DP
type: SiteQuality
SIO_000300: 1.620079e6

QD
type: SiteQuality
SIO_000300: 1.131e1

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

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41819
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2529
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.934984520123839e-4
allele num: 10336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66152
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.681e0

DP
type: SiteQuality
SIO_000300: 1.622832e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 3.71e-1

QD
type: SiteQuality
SIO_000300: 9.01e0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 775
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.474635163307853e-4
allele num: 8634
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 4.446e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.252e1

DP
type: SiteQuality
SIO_000300: 1.622938e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 2522
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66156
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.733102253032929e-4
allele num: 11540
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: 16498
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.338e0

QD
type: SiteQuality
SIO_000300: 1.302e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.61e-1

DP
type: SiteQuality
SIO_000300: 1.622868e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.012e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

GenotypeQuality
all individuals: 1517
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2184
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.426e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.388e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

DP
type: SiteQuality
SIO_000300: 1.622806e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.77e-1

FS
type: SiteQuality
SIO_000300: 6.57e0

QD
type: SiteQuality
SIO_000300: 7.12e0

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

GenotypeQuality
all individuals: 507
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 2522
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41655
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variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
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: 7
allele frequency: 4.242938538004607e-4
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
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: 8632
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 1.622469e6

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

FS
type: SiteQuality
SIO_000300: 5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e-1

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 774
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 21
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41795
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
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: 11540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
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: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66152
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

DP
type: SiteQuality
SIO_000300: 1.622625e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.467e0

VQSLOD
type: SiteQuality
SIO_000300: 3.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.208e1

MQ
type: SiteQuality
SIO_000300: 5.903e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
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: 1.512538947877908e-5
allele num: 66114
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.077e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.807e0

DP
type: SiteQuality
SIO_000300: 1.621692e6

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1513
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51267622678042e-5
allele num: 66108
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: 10310
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.059e0

DP
type: SiteQuality
SIO_000300: 1.621089e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 8.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

BaseQRankSum
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SIO_000300: -5.0e-2

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 2498
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variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
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: 11540
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.924e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.223e1

MQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.107e0

VQSLOD
type: SiteQuality
SIO_000300: 3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

FS
type: SiteQuality
SIO_000300: 8.080000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.620548e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 10304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-5
allele num: 66080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

FS
type: SiteQuality
SIO_000300: 8.222e0

DP
type: SiteQuality
SIO_000300: 1.620217e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.593e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.214e0

QD
type: SiteQuality
SIO_000300: 1.03e1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 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: 1.513408801985592e-5
allele num: 66076
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.79e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.789e0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 1.620222e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66048
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.034e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.199e0

MQ
type: SiteQuality
SIO_000300: 5.669e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.62e0

DP
type: SiteQuality
SIO_000300: 1.619115e6

QD
type: SiteQuality
SIO_000300: 1.305e1

VQSLOD
type: SiteQuality
SIO_000300: -2.212e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 18

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 18
allele frequency: 2.086714583816369e-3
allele num: 8626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66048
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.03e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

DP
type: SiteQuality
SIO_000300: 1.619818e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.171e0