13-27828426-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828426
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828426
    reference: chr 13
allele count: 1
allele frequency: 8.269109913008963e-6
allele num: 120932
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.373T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+8T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+8T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+8T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+8T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+8T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+446T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+8T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+8T>A
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38737
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3199
  bin: 8.25e1
  variant carriers: 0
hgvs: c.129+8T>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

13-27828431-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828431
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828431
    reference: chr 13
allele count: 8
allele frequency: 6.616491605326276e-5
allele num: 120910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+13T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.378T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+13T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+13T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+13T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+13T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+13T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+451T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+13T>C
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7495
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38741
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

13-27828439-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828439
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828439
    reference: chr 13
allele count: 2
allele frequency: 1.654861984510492e-5
allele num: 120856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+21A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+21A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+21A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+21A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.386A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+21A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+21A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+459A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+21A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7220
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

13-27828443-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828443
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828443
    reference: chr 13
allele count: 1
allele frequency: 8.277734549608463e-6
allele num: 120806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+25C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+463C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+25C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+25C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+25C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.390C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+25C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+25C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+25C>T
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

13-27828445-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828445
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828445
    reference: chr 13
allele count: 6
allele frequency: 4.967134129178602e-5
allele num: 120794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+27C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+465C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+27C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+27C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+27C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+27C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.392C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+27C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+27C>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38737
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3515
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2781
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

13-27828446-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828446
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828446
    reference: chr 13
allele count: 1
allele frequency: 8.278968109414843e-6
allele num: 120788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+28T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+28T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+28T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+28T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+28T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+28T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+466T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.393T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+28T>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6239
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3197
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

13-27828447-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828447
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828447
    reference: chr 13
allele count: 1
allele frequency: 8.279379377721846e-6
allele num: 120782
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.394A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+29A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+29A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+29A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+467A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+29A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+29A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+29A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+29A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7975
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2916
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

13-27828449-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828449
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828449
    reference: chr 13
allele count: 2
allele frequency: 1.65604040738594e-5
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+31A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+469A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+31A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.396A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+31A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+31A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+31A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+31A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+31A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7220
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7975
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1889
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP

13-27828450-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828450
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828450
    reference: chr 13
allele count: 755
allele frequency: 6.252173769025655e-3
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.397G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+32G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+470G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+32G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+32G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+32G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+32G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+32G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+32G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 7.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 8.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 7929
  bin: 4.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6224
  bin: 5.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 8.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 5.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 6.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 6.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 7197
  bin: 4.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 3.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 2.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 9.75e1
  variant carriers: 82
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38920
  bin: 9.75e1
  variant carriers: 753
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum

13-27828457-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828457
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828458
    reference: chr 13
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+43dupA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+43dupA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+43dupA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+43dupA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.408dupA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+43dupA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+481dupA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+43dupA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+43dupA
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6244
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3529
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

13-27828458-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828458
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828458
    reference: chr 13
allele count: 31
allele frequency: 2.567755615930025e-4
allele num: 120728
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+40A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+40A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+40A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+40A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+40A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+40A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+478A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+40A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.405A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6243
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3525
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

13-27828465-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828465
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828465
    reference: chr 13
allele count: 3
allele frequency: 2.486654951758894e-5
allele num: 120644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+47G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+47G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.412G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+47G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+47G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+47G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+47G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+485G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+47G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7444
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7238
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3787
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2895
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

13-27828466-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828466
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828465
    reference: chr 13
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+49delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+49delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+487delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+49delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.414delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+49delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+49delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+49delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+49delA
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38647
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: GA
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

13-27828467-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27828467
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27828467
    reference: chr 13
allele count: 1
allele frequency: 8.289124668435012e-6
allele num: 120640
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.129+49A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.129+49A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.129+49A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.129+49A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.141+49A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.129+49A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.67+487A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000473558
  gene symbol: RPL21
  hgvsc: ENST00000473558.1:n.414A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.129+49A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

13-27829153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829153
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829153
    reference: chr 13
allele count: 1
allele frequency: 8.693686644758577e-6
allele num: 115026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-226A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.73A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-226A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-226A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-226A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-226A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-226A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-226A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-226A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5564
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8831
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

13-27829154-A-AAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829154
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829156
    reference: chr 13
allele count: 2
allele frequency: 1.738253750282466e-5
allele num: 115058
alternate allele: AAG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-224_68-223dupAG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-224_142-223dupAG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-224_130-223dupAG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.75_76dupAG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-224_130-223dupAG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-224_130-223dupAG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-224_130-223dupAG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-224_130-223dupAG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-224_130-223dupAG
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/13-27829155-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829155
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829155
    reference: chr 13
allele count: 2
allele frequency: 1.738042269187987e-5
allele num: 115072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-224A>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-224A>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-224A>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-224A>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-224A>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.75A>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-224A>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-224A>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-224A>C
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8333
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1961
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

13-27829157-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829157
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829157
    reference: chr 13
allele count: 1
allele frequency: 8.694140149539211e-6
allele num: 115020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-222C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.77C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-222C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-222C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-222C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-222C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-222C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-222C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-222C>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3062
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

13-27829184-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829184
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829184
    reference: chr 13
allele count: 5
allele frequency: 4.332530371037901e-5
allele num: 115406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-195A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-195A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-195A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-195A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-195A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-195A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.104A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-195A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-195A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4237
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8536
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

13-27829185-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829185
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829185
    reference: chr 13
allele count: 27
allele frequency: 2.338998908467176e-4
allele num: 115434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-194T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.105T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-194T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-194T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-194T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-194T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-194T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-194T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-194T>C
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/13-27829190-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829190
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829190
    reference: chr 13
allele count: 961
allele frequency: 8.316602049293824e-3
allele num: 115552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-189C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-189C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-189C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.110C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-189C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-189C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-189C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-189C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-189C>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7301
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.75e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 5.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 3.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 4.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 9.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 13300
  bin: 3.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 21423
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 4.75e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 6
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/13-27829197-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829197
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829197
    reference: chr 13
allele count: 1
allele frequency: 8.631404502140589e-6
allele num: 115856
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-182C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-182C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.117C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-182C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-182C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-182C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-182C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-182C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-182C>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8705
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

13-27829199-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829199
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829199
    reference: chr 13
allele count: 11
allele frequency: 9.491595623511546e-5
allele num: 115892
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-180C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-180C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-180C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-180C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-180C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-180C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-180C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-180C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.119C>T
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21883
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4345
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

13-27829200-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829200
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829200
    reference: chr 13
allele count: 1
allele frequency: 8.62128422649838e-6
allele num: 115992
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-179G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-179G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-179G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-179G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-179G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-179G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.120G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-179G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-179G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21920
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

13-27829207-ATGATGAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829207
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829200
    reference: chr 13
allele count: 1
allele frequency: 8.583543630152271e-6
allele num: 116502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.130_136delATGACTG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.10_16delATGACTG
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4362
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: ATGATGAC
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

13-27829211-TGAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829211
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829208
    reference: chr 13
allele count: 1
allele frequency: 8.559738414394057e-6
allele num: 116826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.132_134delGAC
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-167_142-165delGAC
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-167_130-165delGAC
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.12_14delGAC
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-167_130-165delGAC
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-167_68-165delGAC
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-167_130-165delGAC
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-167_130-165delGAC
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-167_130-165delGAC
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-167_130-165delGAC
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: TGAC
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ

13-27829212-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829212
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829212
    reference: chr 13
allele count: 198
allele frequency: 1.693436650074409e-3
allele num: 116922
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.12G>A
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-167G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-167G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-167G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-167G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-167G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-167G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-167G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-167G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.132G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 13582
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 4.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21995
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 6.25e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 3
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum

13-27829213-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829213
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829213
    reference: chr 13
allele count: 1
allele frequency: 8.546570261354118e-6
allele num: 117006
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-166A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-166A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.13A>G
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-166A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.133A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-166A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-166A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-166A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-166A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-166A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3260
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

13-27829214-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829214
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829212
    reference: chr 13
allele count: 139
allele frequency: 1.187709344452799e-3
allele num: 117032
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-163_142-162delGT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-163_130-162delGT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-163_68-162delGT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-163_130-162delGT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-163_130-162delGT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-163_130-162delGT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.136_137delGT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.16_17delGT
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-163_130-162delGT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-163_130-162delGT
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7852
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22049
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13595
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 2
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: CTG
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

13-27829215-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829215
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829215
    reference: chr 13
allele count: 1
allele frequency: 8.562376915831835e-6
allele num: 116790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-164T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-164T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-164T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-164T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.135T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-164T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.15T>A
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-164T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-164T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-164T>A
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4368
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

13-27829216-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829216
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829215
    reference: chr 13
allele count: 580
allele frequency: 4.973759132850822e-3
allele num: 116612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-155delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-155delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-155delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-155delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.144delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-155delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.24delT
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-155delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-155delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-155delT
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13602
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 4.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 21960
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 4.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 3.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3194
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1917
  bin: 9.25e1
  variant carriers: 3
num of homozygotes: 17
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: GT
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

13-27829216-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829216
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829217
    reference: chr 13
allele count: 19
allele frequency: 1.629334888347683e-4
allele num: 116612
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-155dupT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-155dupT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.144dupT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.24dupT
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-155dupT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-155dupT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-155dupT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-155dupT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-155dupT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-155dupT
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

13-27829216-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829216
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829216
    reference: chr 13
allele count: 2
allele frequency: 1.715089356155456e-5
allele num: 116612
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21960
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8682
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1917
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26288
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8440
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4273
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3082
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3194
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6586
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 9108
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11436
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 6.215813028344107e-5
  allele num: 16088
  num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

13-27829216-GTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829216
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829214
    reference: chr 13
allele count: 2
allele frequency: 1.715089356155456e-5
allele num: 116612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-156_68-155delTT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-156_130-155delTT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.23_24delTT
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-156_130-155delTT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.143_144delTT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-156_130-155delTT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-156_130-155delTT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-156_130-155delTT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-156_130-155delTT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-156_142-155delTT
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21960
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3194
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: GTT
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

13-27829217-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829217
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829217
    reference: chr 13
allele count: 3
allele frequency: 2.598077422707197e-5
allele num: 115470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-162T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.17T>G
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-162T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.137T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-162T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-162T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-162T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-162T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-162T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-162T>G
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

13-27829220-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829220
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829220
    reference: chr 13
allele count: 4
allele frequency: 3.404776901993497e-5
allele num: 117482
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.20T>G
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-159T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-159T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-159T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-159T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-159T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-159T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-159T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-159T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.140T>G
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22407
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3248
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3158
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

13-27829223-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829223
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829223
    reference: chr 13
allele count: 1
allele frequency: 8.509769215058888e-6
allele num: 117512
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.143T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-156T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-156T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-156T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-156T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-156T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-156T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-156T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.23T>G
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-156T>G
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

13-27829225-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829225
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829225
    reference: chr 13
allele count: 1
allele frequency: 8.500510030601837e-6
allele num: 117640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-154G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-154G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-154G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.25G>T
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-154G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-154G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-154G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-154G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.145G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-154G>T
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

13-27829226-A-ATTGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829226
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829230
    reference: chr 13
allele count: 1
allele frequency: 8.494011721736177e-6
allele num: 117730
alternate allele: ATTGC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-149_130-146dupCTTG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-149_142-146dupCTTG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-149_130-146dupCTTG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-149_130-146dupCTTG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-149_130-146dupCTTG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-149_130-146dupCTTG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-149_130-146dupCTTG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-149_68-146dupCTTG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.30_33dupCTTG
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.150_153dupCTTG
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/13-27829247-AAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829247
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829245
    reference: chr 13
allele count: 1
allele frequency: 8.430992327796981e-6
allele num: 118610
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-128_130-127delCA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.51_52delCA
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-128_130-127delCA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-128_130-127delCA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-128_130-127delCA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-128_130-127delCA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-128_130-127delCA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.171_172delCA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-128_68-127delCA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-128_142-127delCA
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: AAC
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

13-27829252-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829252
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829252
    reference: chr 13
allele count: 18
allele frequency: 1.516325774168548e-4
allele num: 118708
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.52A>G
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-127A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.172A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-127A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-127A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-127A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-127A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-127A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-127A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-127A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22358
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4347
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

13-27829254-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829254
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829254
    reference: chr 13
allele count: 1
allele frequency: 8.424599831508003e-6
allele num: 118700
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-125T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.54T>A
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-125T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-125T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-125T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-125T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-125T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.174T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-125T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-125T>A
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3237
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8204
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP

13-27829257-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829257
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829257
    reference: chr 13
allele count: 1
allele frequency: 8.421478137842754e-6
allele num: 118744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.177A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.57A>G
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-122A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-122A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-122A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-122A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-122A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-122A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-122A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-122A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8845
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

13-27829259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829259
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829259
    reference: chr 13
allele count: 5
allele frequency: 4.209959079197751e-5
allele num: 118766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-120C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.179C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-120C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-120C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-120C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-120C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-120C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.59C>T
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-120C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-120C>T
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22127
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

13-27829261-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829261
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829261
    reference: chr 13
allele count: 1
allele frequency: 8.420201748033883e-6
allele num: 118762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-118G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-118G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-118G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.181G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-118G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-118G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.61G>T
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-118G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-118G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-118G>T
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13146
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3177
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

13-27829270-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829270
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829270
    reference: chr 13
allele count: 20
allele frequency: 1.683303314424226e-4
allele num: 118814
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207500
  ensembl transcript: ENST00000384769
  gene symbol: SNORD102
  hgvsc: ENST00000384769.1:n.70G>C
  variant of: http://identifiers.org/hgnc/10099
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.190G>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-109G>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-109G>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-109G>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-109G>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-109G>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-109G>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-109G>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-109G>C
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8788
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12646
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8189
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

13-27829274-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829274
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829275
    reference: chr 13
allele count: 2
allele frequency: 1.683615058253081e-5
allele num: 118792
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-105_68-104insA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-105_130-104insA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-105_130-104insA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-105_130-104insA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-105_130-104insA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-105_130-104insA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.194_195insA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-105_142-104insA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-105_130-104insA
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20776
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/13-27829283-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829283
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829283
    reference: chr 13
allele count: 1
allele frequency: 8.422187410514259e-6
allele num: 118734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-96C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-96C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-96C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-96C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-96C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-96C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-96C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.203C>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-96C>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11239
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22581
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2524
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

13-27829288-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829288
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829287
    reference: chr 13
allele count: 9
allele frequency: 7.580990245792551e-5
allele num: 118718
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-88delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-88delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-88delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-88delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-88delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-88delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.211delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-88delA
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-88delA
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9777
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10627
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4012
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2571
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21123
  bin: 6.25e1
  variant carriers: 0
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: GA
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

13-27829310-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829310
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829310
    reference: chr 13
allele count: 118701
allele frequency: 9.950624528460056e-1
allele num: 119290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-69G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-69G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-69G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-69G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.230G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-69G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-69G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-69G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-69G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 9.75e1
  variant carriers: 3178
genotype depth: GenotypeDepth
  all individuals: 9818
  bin: 2.25e1
  variant carriers: 9815
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 7.5e0
  variant carriers: 894
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.25e1
  variant carriers: 546
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 1.25e1
  variant carriers: 2703
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 2.75e1
  variant carriers: 10345
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 6.75e1
  variant carriers: 1008
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 5.25e1
  variant carriers: 1513
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.75e1
  variant carriers: 658
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 1219
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 7.25e1
  variant carriers: 1048
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 3.75e1
  variant carriers: 5212
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 4.25e1
  variant carriers: 3072
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 1.75e1
  variant carriers: 6539
genotype depth: GenotypeDepth
  all individuals: 8001
  bin: 3.25e1
  variant carriers: 7998
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 4.75e1
  variant carriers: 1973
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.25e1
  variant carriers: 1125
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.75e1
  variant carriers: 897
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 8.25e1
  variant carriers: 815
genotype quality: GenotypeQuality
  all individuals: 3581
  bin: 6.25e1
  variant carriers: 3578
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 782
  bin: 4.25e1
  variant carriers: 782
genotype quality: GenotypeQuality
  all individuals: 26908
  bin: 9.75e1
  variant carriers: 26908
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 2.75e1
  variant carriers: 303
num of homozygotes: 59065
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

13-27829311-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829311
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829311
    reference: chr 13
allele count: 3
allele frequency: 2.537212449255751e-5
allele num: 118240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-68C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-68C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-68C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-68C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-68C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-68C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-68C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-68C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.231C>T
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11529
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16471
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

13-27829313-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829313
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829313
    reference: chr 13
allele count: 1
allele frequency: 8.472135147499873e-6
allele num: 118034
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-66G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-66G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.233G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-66G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-66G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-66G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-66G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-66G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-66G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10675
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6822
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2477
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

13-27829319-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829319
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829319
    reference: chr 13
allele count: 1
allele frequency: 8.469838903664053e-6
allele num: 118066
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-60T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-60T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-60T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-60T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.239T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-60T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-60T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-60T>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-60T>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10838
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9571
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2707
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1800
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

13-27829329-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829329
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829328
    reference: chr 13
allele count: 3
allele frequency: 2.543752543752544e-5
allele num: 117936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-46delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-46delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-46delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-46delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.253delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-46delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-46delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-46delT
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-46delT
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12217
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1781
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17285
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: AT
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

13-27829336-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829336
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829336
    reference: chr 13
allele count: 1
allele frequency: 8.475438180153914e-6
allele num: 117988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-43A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-43A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-43A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-43A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-43A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-43A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-43A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.256A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-43A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13108
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19322
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3095
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

13-27829336-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829336
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829335
    reference: chr 13
allele count: 4
allele frequency: 3.390175272061565e-5
allele num: 117988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-41delG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.258delG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-41delG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-41delG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-41delG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-41delG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-41delG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-41delG
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-41delG
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15625
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13108
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19322
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2520
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2347
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: AG
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

13-27829342-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829342
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829342
    reference: chr 13
allele count: 1
allele frequency: 8.472996559963397e-6
allele num: 118022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-37G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.262G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-37G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-37G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-37G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-37G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-37G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-37G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-37G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8629
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20120
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3434
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

13-27829343-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829343
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829343
    reference: chr 13
allele count: 1
allele frequency: 8.474001762592366e-6
allele num: 118008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-36G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-36G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-36G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.263G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-36G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-36G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-36G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-36G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-36G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15857
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2565
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20912
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7115
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD

13-27829350-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829350
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829350
    reference: chr 13
allele count: 2
allele frequency: 1.691961490956466e-5
allele num: 118206
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-29C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-29C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-29C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-29C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-29C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-29C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.270C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-29C>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-29C>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16093
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16291
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7420
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

13-27829352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829352
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829352
    reference: chr 13
allele count: 1
allele frequency: 8.455658526686058e-6
allele num: 118264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-27G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-27G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-27G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-27G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-27G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.272G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-27G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-27G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-27G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16476
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24813
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

13-27829356-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829356
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829356
    reference: chr 13
allele count: 1
allele frequency: 8.431561019207096e-6
allele num: 118602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-23T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-23T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.276T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-23T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-23T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-23T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-23T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-23T>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-23T>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7850
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3758
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ

13-27829364-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829364
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829364
    reference: chr 13
allele count: 2
allele frequency: 1.678274733573886e-5
allele num: 119170
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-15T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-15T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-15T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.284T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-15T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-15T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-15T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-15T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-15T>C
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28803
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum

13-27829365-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829365
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829365
    reference: chr 13
allele count: 1
allele frequency: 8.388558006878617e-6
allele num: 119210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-14G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-14G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-14G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-14G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-14G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-14G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-14G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-14G>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.285G>T
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19844
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

13-27829366-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829366
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829366
    reference: chr 13
allele count: 6
allele frequency: 5.027062352330043e-5
allele num: 119354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-13G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-13G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-13G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-13G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.286G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-13G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-13G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-13G>A
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-13G>A
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20006
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17470
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8266
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3943
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS

13-27829373-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829373
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829373
    reference: chr 13
allele count: 3
allele frequency: 2.499500099980004e-5
allele num: 120024
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.142-6T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.130-6T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.130-6T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.130-6T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.130-6T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.293T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.68-6T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.130-6T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.130-6T>C
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17833
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9789
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5723
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
hgvs: c.130-6T>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

13-27829381-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829381
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829381
    reference: chr 13
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.132A>G
  hgvsp: ENST00000326092.4:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.144A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.132A>G
  hgvsp: ENST00000272274.4:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.132A>G
  hgvsp: ENST00000493317.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.70A>G
  hgvsp: ENSP00000473246.1:p.Asn24Asp
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.132A>G
  hgvsp: ENST00000319826.4:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.132A>G
  hgvsp: ENST00000461690.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.132A>G
  hgvsp: ENST00000311549.6:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.301A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn24Asp
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

13-27829383-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829383
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829383
    reference: chr 13
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.134T>C
  hgvsp: ENSP00000434298.1:p.Met45Thr
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.134T>C
  hgvsp: ENSP00000351021.2:p.Met45Thr
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.134T>C
  hgvsp: ENSP00000370574.1:p.Met45Thr
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.134T>C
  hgvsp: ENSP00000370569.1:p.Met45Thr
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.134T>C
  hgvsp: ENSP00000346027.4:p.Met45Thr
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.303T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.146T>C
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.134T>C
  hgvsp: ENSP00000471695.1:p.Met45Thr
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.72T>C
  hgvsp: ENST00000483765.1:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Met45Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

13-27829403-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829403
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829403
    reference: chr 13
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.92A>G
  hgvsp: ENSP00000473246.1:p.Asn31Ser
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.154A>G
  hgvsp: ENSP00000346027.4:p.Met52Val
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.154A>G
  hgvsp: ENSP00000370574.1:p.Met52Val
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.323A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.154A>G
  hgvsp: ENSP00000370569.1:p.Met52Val
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.154A>G
  hgvsp: ENSP00000471695.1:p.Met52Val
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.154A>G
  hgvsp: ENSP00000434298.1:p.Met52Val
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.166A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.154A>G
  hgvsp: ENSP00000351021.2:p.Met52Val
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Met52Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

13-27829408-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829408
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829408
    reference: chr 13
allele count: 619
allele frequency: 5.105912630328626e-3
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.159C>T
  hgvsp: ENST00000326092.4:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.159C>T
  hgvsp: ENST00000461690.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.159C>T
  hgvsp: ENST00000493317.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.171C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.97C>T
  hgvsp: ENSP00000473246.1:p.Pro33Ser
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.159C>T
  hgvsp: ENST00000311549.6:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.159C>T
  hgvsp: ENST00000319826.4:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.328C>T
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.159C>T
  hgvsp: ENST00000272274.4:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 3.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 20941
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 18646
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 4.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 10500
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 6.25e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro33Ser
num of homozygotes: 18
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD

13-27829443-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27829443
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 27829443
    reference: chr 13
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370569
  ensembl transcript: ENST00000326092
  gene symbol: RPL21
  hgvsc: ENST00000326092.4:c.194A>G
  hgvsp: ENSP00000370569.1:p.Tyr65Cys
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000471695
  ensembl transcript: ENST00000493317
  gene symbol: RPL21
  hgvsc: ENST00000493317.1:c.194A>G
  hgvsp: ENSP00000471695.1:p.Tyr65Cys
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000473246
  ensembl transcript: ENST00000483765
  gene symbol: RPL21
  hgvsc: ENST00000483765.1:c.132A>G
  hgvsp: ENST00000483765.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000351021
  ensembl transcript: ENST00000272274
  gene symbol: RPL21
  hgvsc: ENST00000272274.4:c.194A>G
  hgvsp: ENSP00000351021.2:p.Tyr65Cys
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000346027
  ensembl transcript: ENST00000311549
  gene symbol: RPL21
  hgvsc: ENST00000311549.6:c.194A>G
  hgvsp: ENSP00000346027.4:p.Tyr65Cys
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000370574
  ensembl transcript: ENST00000319826
  gene symbol: RPL21
  hgvsc: ENST00000319826.4:c.194A>G
  hgvsp: ENSP00000370574.1:p.Tyr65Cys
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000122026
  ensembl protein: ENSP00000434298
  ensembl transcript: ENST00000461690
  gene symbol: RPL21
  hgvsc: ENST00000461690.1:c.194A>G
  hgvsp: ENSP00000434298.1:p.Tyr65Cys
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000485756
  gene symbol: RPL21
  hgvsc: ENST00000485756.1:n.363A>G
  variant of: http://identifiers.org/hgnc/10313
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000122026
  ensembl transcript: ENST00000466550
  gene symbol: RPL21
  hgvsc: ENST00000466550.1:n.206A>G
  variant of: http://identifiers.org/hgnc/10313
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20901
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr65Cys
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5348
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2931
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 265
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2888
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3519
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

MQ
type: SiteQuality
SIO_000300: 5.926e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: -2.436e-1

FS
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SIO_000300: 1.075e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.69e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.981403e6

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

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

East Asian
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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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

South Asian
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allele frequency: 4.847897224578839e-4
allele num: 16502
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.883e1

BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.980834e6

QD
type: SiteQuality
SIO_000300: 1.245e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.49e-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: 2

South Asian
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allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8646
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: 11572
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.978455e6

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.54e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.153e1

FS
type: SiteQuality
SIO_000300: 8.01e-1

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

MQ
type: SiteQuality
SIO_000300: 5.775e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.297e0

ReadPosRankSum
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DP
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ClippingRankSum
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SIO_000300: -1.773e0

FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.93e1

VQSLOD
type: SiteQuality
SIO_000300: 3.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9998
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: 6
allele frequency: 9.013339742819372e-5
allele num: 66568
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
type: SiteQuality
SIO_000300: 1.454e1

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: 1

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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BaseQRankSum
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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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bin: 7.25e1
variant carriers: 0

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

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

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

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

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

African
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allele frequency: 1.001001001001001e-4
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DP
type: SiteQuality
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BaseQRankSum
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MQ
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ReadPosRankSum
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FS
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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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: 66562
num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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Other
type: Population
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allele num: 906
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South Asian
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allele num: 16500
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East Asian
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allele count: 0
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European (Finnish)
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allele num: 6614
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MQ
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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FS
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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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variant carriers: 0

African
type: Population
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allele frequency: 1.102425335738625e-3
allele num: 9978
num of homozygotes: 0

South Asian
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allele count: 19
allele frequency: 1.151515151515151e-3
allele num: 16500
num of homozygotes: 0

Latino
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allele count: 22
allele frequency: 1.90179806362379e-3
allele num: 11568
num of homozygotes: 0

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

Other
type: Population
allele count: 7
allele frequency: 7.72626931567329e-3
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.663138796492289e-3
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 684
allele frequency: 1.02773687531929e-2
allele num: 66554
num of homozygotes: 1

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9956
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.970123e6

QD
type: SiteQuality
SIO_000300: 1.16e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.479e0

GenotypeQuality
all individuals: 2723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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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GenotypeQuality
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variant carriers: 30

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.507617874207411e-5
allele num: 66554
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 23
allele frequency: 2.309236947791165e-3
allele num: 9960
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: 3
allele frequency: 2.594258042199931e-4
allele num: 11564
num of homozygotes: 1

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.38e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.614e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

DP
type: SiteQuality
SIO_000300: 2.970275e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

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
all individuals: 3186
bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

FS
type: SiteQuality
SIO_000300: 1.621e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 1.591e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 3.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.23e-1

DP
type: SiteQuality
SIO_000300: 2.966779e6

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 2.261e0

DP
type: SiteQuality
SIO_000300: 2.966349e6

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

QD
type: SiteQuality
SIO_000300: 1.382e1

MQ
type: SiteQuality
SIO_000300: 6.008e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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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: 100
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2890
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variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 4.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66508
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: 8618
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.00664384940608e-4
allele num: 9934
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.122e-1

QD
type: SiteQuality
SIO_000300: 1.465e1

DP
type: SiteQuality
SIO_000300: 2.966099e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.059e0

MQRankSum
type: SiteQuality
SIO_000300: -9.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 7.868e0

MQ
type: SiteQuality
SIO_000300: 5.806e1

GenotypeQuality
all individuals: 4131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
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variant carriers: 0

GenotypeQuality
all individuals: 23542
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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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GenotypeQuality
all individuals: 790
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variant carriers: 0

GenotypeQuality
all individuals: 2998
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.589269253997012e-5
allele num: 62922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
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: -3.13e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.554e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

FS
type: SiteQuality
SIO_000300: 2.829e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 1.910607e6

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: 2

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.747030048916841e-4
allele num: 11448
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8656
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.011e1

MQRankSum
type: SiteQuality
SIO_000300: 2.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.63e-1

DP
type: SiteQuality
SIO_000300: 1.910848e6

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 501
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16232
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.177427554651754e-5
allele num: 62944
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.4e-1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 7.68e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.91131e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 640
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.589016716455857e-5
allele num: 62932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16198
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.29e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

VQSLOD
type: SiteQuality
SIO_000300: 3.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.929e0

MQRankSum
type: SiteQuality
SIO_000300: 2.36e-1

DP
type: SiteQuality
SIO_000300: 1.911974e6

QD
type: SiteQuality
SIO_000300: 1.047e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

GenotypeQuality
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bin: 2.75e1
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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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1976
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.922674694977024e-5
allele num: 63110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8708
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

DP
type: SiteQuality
SIO_000300: 1.933267e6

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-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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variant carriers: 27

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1401
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 27
allele frequency: 3.097040605643496e-3
allele num: 8718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63120
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

DP
type: SiteQuality
SIO_000300: 1.934019e6

QD
type: SiteQuality
SIO_000300: 1.241e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.936e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 951

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 4215
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1939
bin: 9.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 682
allele frequency: 1.079045630023416e-2
allele num: 63204
num of homozygotes: 5

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 2.173913043478261e-3
allele num: 8740
num of homozygotes: 0

South Asian
type: Population
allele count: 67
allele frequency: 4.097358121330724e-3
allele num: 16352
num of homozygotes: 0

Latino
type: Population
allele count: 48
allele frequency: 4.190675746464118e-3
allele num: 11454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 140
allele frequency: 2.12636695018226e-2
allele num: 6584
num of homozygotes: 1

Other
type: Population
allele count: 5
allele frequency: 5.773672055427252e-3
allele num: 866
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.424e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 1.954595e6

FS
type: SiteQuality
SIO_000300: 1.134e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

QD
type: SiteQuality
SIO_000300: 1.126e1

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 136
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 78
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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
all individuals: 26183
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variant carriers: 0

GenotypeQuality
all individuals: 3132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.0960741282614e-5
allele num: 16404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8812
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.136e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.489e0

FS
type: SiteQuality
SIO_000300: 6.345e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.598e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

DP
type: SiteQuality
SIO_000300: 1.927238e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

QD
type: SiteQuality
SIO_000300: 1.136e1

GenotypeQuality
all individuals: 156
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variant carriers: 0

GenotypeQuality
all individuals: 3234
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GenotypeQuality
all individuals: 113
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 127
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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: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 1978
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.154375118289067e-5
allele num: 63404
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.366049598323437e-4
allele num: 11452
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.53514739229025e-4
allele num: 8820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.928497e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

QD
type: SiteQuality
SIO_000300: 1.037e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

FS
type: SiteQuality
SIO_000300: 3.281e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 70
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GenotypeQuality
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GenotypeQuality
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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: 3141
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variant carriers: 0

GenotypeQuality
all individuals: 1982
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variant carriers: 0

GenotypeQuality
all individuals: 4350
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575646803012637e-5
allele num: 63466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8844
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.111e0

QD
type: SiteQuality
SIO_000300: 9.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

FS
type: SiteQuality
SIO_000300: 2.807e0

DP
type: SiteQuality
SIO_000300: 1.929934e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3253
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GenotypeQuality
all individuals: 15
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566661444461852e-5
allele num: 63830
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.935721e6

MQRankSum
type: SiteQuality
SIO_000300: -4.183e0

MQ
type: SiteQuality
SIO_000300: 5.227e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 2.995e0

VQSLOD
type: SiteQuality
SIO_000300: 8.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 37
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GenotypeQuality
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GenotypeQuality
all individuals: 3260
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 26590
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GenotypeQuality
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GenotypeQuality
all individuals: 97
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GenotypeQuality
all individuals: 114
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GenotypeQuality
all individuals: 1984
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GenotypeQuality
all individuals: 31
bin: 4.75e1
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GenotypeQuality
all individuals: 8784
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GenotypeQuality
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GenotypeQuality
all individuals: 1412
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4364
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.106439477760567e-4
allele num: 9038
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

DP
type: SiteQuality
SIO_000300: 1.939631e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

VQSLOD
type: SiteQuality
SIO_000300: 4.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 6.998e0

MQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4358
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8779
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8433
bin: 9.75e1
variant carriers: 195

GenotypeQuality
all individuals: 1288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3151
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26626
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9054
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.149425287356322e-3
allele num: 870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

South Asian
type: Population
allele count: 197
allele frequency: 1.199318154145866e-2
allele num: 16426
num of homozygotes: 3

DP
type: SiteQuality
SIO_000300: 1.94468e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.629e0

FS
type: SiteQuality
SIO_000300: 1.107e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

QD
type: SiteQuality
SIO_000300: 1.126e1

MQ
type: SiteQuality
SIO_000300: 5.929e1

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

GenotypeQuality
all individuals: 4377
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26718
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 716
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8307
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9066
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557195801800118e-5
allele num: 64218
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.942043e6

VQSLOD
type: SiteQuality
SIO_000300: -8.437e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

QD
type: SiteQuality
SIO_000300: 1.338e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.612e0

FS
type: SiteQuality
SIO_000300: 9.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.54e-1

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3256
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8787
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8420
bin: 9.75e1
variant carriers: 137

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26628
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4368
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3151
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.617801047120419e-4
allele num: 11460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.783070265558357e-5
allele num: 64242
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.104728236853734e-4
allele num: 9052
num of homozygotes: 0

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

South Asian
type: Population
allele count: 130
allele frequency: 7.906580707943072e-3
allele num: 16442
num of homozygotes: 2

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

QD
type: SiteQuality
SIO_000300: 1.618e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

FS
type: SiteQuality
SIO_000300: 5.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

DP
type: SiteQuality
SIO_000300: 1.945789e6

BaseQRankSum
type: SiteQuality
SIO_000300: -9.4e-2

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3258
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1414
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1209
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8280
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3152
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.104972375690608e-4
allele num: 9050
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16186
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.04e-1

FS
type: SiteQuality
SIO_000300: 2.709e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.235e0

DP
type: SiteQuality
SIO_000300: 1.9377e6

QD
type: SiteQuality
SIO_000300: 4.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

VQSLOD
type: SiteQuality
SIO_000300: -2.326e0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 193
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 26288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 727
bin: 7.5e0
variant carriers: 6

GenotypeQuality
all individuals: 8682
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8440
bin: 9.75e1
variant carriers: 549

GenotypeQuality
all individuals: 3082
bin: 8.25e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.792531637678449e-5
allele num: 64164
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.196458482890644e-4
allele num: 8358
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.107906514172054e-4
allele num: 16088
num of homozygotes: 0

African
type: Population
allele count: 529
allele frequency: 5.808080808080808e-2
allele num: 9108
num of homozygotes: 17

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

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

Latino
type: Population
allele count: 40
allele frequency: 3.497726477789437e-3
allele num: 11436
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.958053e6

QD
type: SiteQuality
SIO_000300: 1.226e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1917
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3194
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8440
bin: 9.75e1
variant carriers: 19

East Asian
type: Population
allele count: 1
allele frequency: 1.196458482890644e-4
allele num: 8358
num of homozygotes: 0

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

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

African
type: Population
allele count: 14
allele frequency: 1.537110232762407e-3
allele num: 9108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.11701265507138e-5
allele num: 64164
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.748863238894718e-4
allele num: 11436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16088
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.04e0

DP
type: SiteQuality
SIO_000300: 1.958053e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55850632753569e-5
allele num: 64164
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: 1.958053e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.226e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

GenotypeQuality
all individuals: 144
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 727
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8440
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8682
bin: 6.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.748863238894718e-4
allele num: 11436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64164
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.26e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

MQRankSum
type: SiteQuality
SIO_000300: 4.83e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

DP
type: SiteQuality
SIO_000300: 1.958053e6

GenotypeQuality
all individuals: 314
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7864
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 137
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26290
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3171
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1383
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.816787162757891e-5
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.116624072804338e-5
allele num: 64172
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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QD
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SIO_000300: 1.266e1

BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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MQ
type: SiteQuality
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ReadPosRankSum
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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GenotypeQuality
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GenotypeQuality
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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

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

African
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allele count: 1
allele frequency: 1.090037061260083e-4
allele num: 9174
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 64540
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Latino
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allele frequency: 2.6168876482903e-4
allele num: 11464
num of homozygotes: 0

MQRankSum
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MQ
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FS
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

African
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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: 64554
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

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

Latino
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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

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

Latino
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allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64652
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.08483402039488e-4
allele num: 9218
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 2.357e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.266e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
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SIO_000300: 3.3e-1

DP
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.191043353978085e-4
allele num: 8396
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64714
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Other
type: Population
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.098e0

MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

DP
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.793e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 65356
num of homozygotes: 0

Other
type: Population
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East Asian
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allele count: 1
allele frequency: 1.191327138432213e-4
allele num: 8394
num of homozygotes: 0

European (Finnish)
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South Asian
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African
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Latino
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ClippingRankSum
type: SiteQuality
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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QD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16456
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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allele num: 65428
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Latino
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Other
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MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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MQRankSum
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FS
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VQSLOD
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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African
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Latino
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East Asian
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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MQ
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QD
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527463799107961e-5
allele num: 65468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.939587e6

QD
type: SiteQuality
SIO_000300: 1.281e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 7.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.04e-1

GenotypeQuality
all individuals: 4308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1939
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3211
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1300
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8187
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 292
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26904
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8796
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.619629758994062e-4
allele num: 11452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.082725060827251e-5
allele num: 16440
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527090587013621e-5
allele num: 65484
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.938924e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

FS
type: SiteQuality
SIO_000300: 3.625e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

QD
type: SiteQuality
SIO_000300: 1.383e1

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 131
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4268
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8184
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65478
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.199328376109379e-4
allele num: 8338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.452e-1

DP
type: SiteQuality
SIO_000300: 1.929174e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.414e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.91e-1

GenotypeQuality
all individuals: 603
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1927
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3100
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8331
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26119
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8306
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.042102701387199e-4
allele num: 16436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9688
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.745845723281441e-5
allele num: 11434
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.13792682181907e-4
allele num: 65484
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.914625e6

QD
type: SiteQuality
SIO_000300: 1.472e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.36e-1

FS
type: SiteQuality
SIO_000300: 1.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.91e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.3e-2

GenotypeQuality
all individuals: 1405
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25383
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8175
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4187
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3086
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3090
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.217433649866082e-4
allele num: 16428
num of homozygotes: 0

African
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: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.747e0

MQ
type: SiteQuality
SIO_000300: 5.817e1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 1.900305e6

QD
type: SiteQuality
SIO_000300: 1.807e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.48e-1

GenotypeQuality
all individuals: 1411
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8160
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1916
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4079
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1423
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7632
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528771479239283e-5
allele num: 65412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.8e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.243e0

FS
type: SiteQuality
SIO_000300: 7.791e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

QD
type: SiteQuality
SIO_000300: 1.335e1

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.74e-1

DP
type: SiteQuality
SIO_000300: 1.858738e6

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2902
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1902
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1907
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7373
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8167
bin: 9.75e1
variant carriers: 9

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

African
type: Population
allele count: 9
allele frequency: 9.129640900791236e-4
allele num: 9858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65370
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.398e1

FS
type: SiteQuality
SIO_000300: 8.898999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

MQ
type: SiteQuality
SIO_000300: 5.837e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
type: SiteQuality
SIO_000300: 1.838065e6

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 6

GenotypeQuality
all individuals: 1164
bin: 3.75e1
variant carriers: 1164

GenotypeQuality
all individuals: 408
bin: 2.25e1
variant carriers: 408

GenotypeQuality
all individuals: 3994
bin: 8.25e1
variant carriers: 3994

GenotypeQuality
all individuals: 216
bin: 1.75e1
variant carriers: 216

GenotypeQuality
all individuals: 2158
bin: 7.25e1
variant carriers: 2158

GenotypeQuality
all individuals: 4252
bin: 7.75e1
variant carriers: 4250

GenotypeQuality
all individuals: 792
bin: 3.25e1
variant carriers: 792

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 42

GenotypeQuality
all individuals: 2073
bin: 4.75e1
variant carriers: 2072

GenotypeQuality
all individuals: 2771
bin: 5.25e1
variant carriers: 2771

GenotypeQuality
all individuals: 1677
bin: 5.75e1
variant carriers: 1677

GenotypeQuality
all individuals: 2009
bin: 8.75e1
variant carriers: 2008

GenotypeQuality
all individuals: 3436
bin: 9.25e1
variant carriers: 3435

GenotypeQuality
all individuals: 4023
bin: 6.75e1
variant carriers: 4022

East Asian
type: Population
allele count: 8214
allele frequency: 1.0e0
allele num: 8214
num of homozygotes: 4107

European (Non-Finnish)
type: Population
allele count: 65468
allele frequency: 9.99694600537503e-1
allele num: 65488
num of homozygotes: 32724

European (Finnish)
type: Population
allele count: 6576
allele frequency: 1.0e0
allele num: 6576
num of homozygotes: 3288

Other
type: Population
allele count: 893
allele frequency: 9.988814317673378e-1
allele num: 894
num of homozygotes: 446

African
type: Population
allele count: 9710
allele frequency: 9.467628705148206e-1
allele num: 10256
num of homozygotes: 4591

Latino
type: Population
allele count: 11410
allele frequency: 9.98075577326802e-1
allele num: 11432
num of homozygotes: 5694

South Asian
type: Population
allele count: 16430
allele frequency: 1.0e0
allele num: 16430
num of homozygotes: 8215

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.12e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

DP
type: SiteQuality
SIO_000300: 2.451159e6

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQ
type: SiteQuality
SIO_000300: 5.798e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 3.467e1

GenotypeQuality
all individuals: 1956
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3667
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2517
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9257
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2193
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2440
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3242
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5312
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8114
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.113964294448521e-5
allele num: 16356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.086705559156712e-5
allele num: 64794
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.509e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.069e0

MQRankSum
type: SiteQuality
SIO_000300: 5.19e-1

MQ
type: SiteQuality
SIO_000300: 5.734e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

QD
type: SiteQuality
SIO_000300: 1.207e1

DP
type: SiteQuality
SIO_000300: 2.369167e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.298e0

GenotypeQuality
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bin: 7.25e1
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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bin: 1.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.234263144902493e-4
allele num: 8102
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64646
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.239e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.271e0

BaseQRankSum
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SIO_000300: -3.033e0

MQRankSum
type: SiteQuality
SIO_000300: -2.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-1

MQ
type: SiteQuality
SIO_000300: 5.701e1

DP
type: SiteQuality
SIO_000300: 2.361801e6

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: 8.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547173314354674e-5
allele num: 64634
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

DP
type: SiteQuality
SIO_000300: 2.361052e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.32e-1

FS
type: SiteQuality
SIO_000300: 9.625999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQ
type: SiteQuality
SIO_000300: 5.672e1

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.617e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.49e-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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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.649432769202157e-5
allele num: 64524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8110
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

FS
type: SiteQuality
SIO_000300: 4.798e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

QD
type: SiteQuality
SIO_000300: 1.093e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.587e1

DP
type: SiteQuality
SIO_000300: 1.661886e6

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
all individuals: 1085
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.817396426467701e-5
allele num: 10186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 8.74e-1

QD
type: SiteQuality
SIO_000300: 1.454e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

FS
type: SiteQuality
SIO_000300: 4.023e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

DP
type: SiteQuality
SIO_000300: 1.66346e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

MQ
type: SiteQuality
SIO_000300: 5.799e1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64562
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11304
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African
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allele frequency: 3.926958570587081e-4
allele num: 10186
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

South Asian
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allele num: 16368
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8118
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.547987616099071e-5
allele num: 64600
num of homozygotes: 0

African
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
type: Population
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DP
type: SiteQuality
SIO_000300: 1.673329e6

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.579e1

MQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
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num of homozygotes: 0

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

Other
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Latino
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allele frequency: 8.846426043878273e-5
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East Asian
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South Asian
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European (Finnish)
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MQ
type: SiteQuality
SIO_000300: 5.443e1

MQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
type: SiteQuality
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DP
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.223e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele num: 10192
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544735541275334e-5
allele num: 64736
num of homozygotes: 0

East Asian
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Other
type: Population
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Latino
type: Population
allele count: 1
allele frequency: 8.833922261484099e-5
allele num: 11320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.05e-1

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

DP
type: SiteQuality
SIO_000300: 1.696679e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.64e-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: 8.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
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: 1
allele frequency: 1.224589762429586e-4
allele num: 8166
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64762
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.558e0

MQ
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SIO_000300: 5.554e1

DP
type: SiteQuality
SIO_000300: 1.704834e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.59e-1

QD
type: SiteQuality
SIO_000300: 1.713e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.919e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53907716932927e-5
allele num: 64974
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.97e0

FS
type: SiteQuality
SIO_000300: 1.0656e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

DP
type: SiteQuality
SIO_000300: 1.717747e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.333e0

QD
type: SiteQuality
SIO_000300: 1.285e1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

MQ
type: SiteQuality
SIO_000300: 5.811e1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.522997258604935e-4
allele num: 6566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65324
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.093845216331505e-5
allele num: 16410
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.76e-1

DP
type: SiteQuality
SIO_000300: 1.746295e6

VQSLOD
type: SiteQuality
SIO_000300: -9.399999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.684e1

QD
type: SiteQuality
SIO_000300: 1.488e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530409231428484e-5
allele num: 65342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
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: 894
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.732e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.286e0

FS
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 1.750216e6

VQSLOD
type: SiteQuality
SIO_000300: -1.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 7.13e0

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

Latino
type: Population
allele count: 2
allele frequency: 1.751313485113835e-4
allele num: 11420
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.923406743324888e-4
allele num: 10262
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65406
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.782e0

MQ
type: SiteQuality
SIO_000300: 5.549e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.753201e6

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65832
num of homozygotes: 0

African
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allele frequency: 9.712509712509713e-5
allele num: 10296
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Latino
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South Asian
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allele count: 2
allele frequency: 1.215214485356665e-4
allele num: 16458
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East Asian
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VQSLOD
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.47e-1

ClippingRankSum
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SIO_000300: 2.57e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.698e1

MQ
type: SiteQuality
SIO_000300: 5.887e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66198
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South Asian
type: Population
allele count: 0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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FS
type: SiteQuality
SIO_000300: 8.429e0

InbreedingCoeff
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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SIO_000300: 1.790649e6

BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
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allele num: 16486
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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VQSLOD
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 3.22e0

MQ
type: SiteQuality
SIO_000300: 5.339e1

GenotypeQuality
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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: 1610
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3105
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3530
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9021
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5764
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1247
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 9.71e-1

DP
type: SiteQuality
SIO_000300: 1.809496e6

VQSLOD
type: SiteQuality
SIO_000300: -1.439e0

FS
type: SiteQuality
SIO_000300: 1.625e0

QD
type: SiteQuality
SIO_000300: 1.603e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e-1

MQ
type: SiteQuality
SIO_000300: 4.73e1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.178e0

GenotypeQuality
all individuals: 4292
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6195
bin: 9.75e1
variant carriers: 601

GenotypeQuality
all individuals: 8992
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31508
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3502
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 113
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1586
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

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

Latino
type: Population
allele count: 40
allele frequency: 3.460806367883717e-3
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.501260352898812e-5
allele num: 66648
num of homozygotes: 0

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

African
type: Population
allele count: 573
allele frequency: 5.531955976057154e-2
allele num: 10358
num of homozygotes: 18

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.360000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.25e-1

DP
type: SiteQuality
SIO_000300: 1.829395e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

MQ
type: SiteQuality
SIO_000300: 4.593e1

FS
type: SiteQuality
SIO_000300: 5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

QD
type: SiteQuality
SIO_000300: 1.454e1