9-136307729-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307729
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307729
    reference: chr 9
allele count: 2
allele frequency: 1.665306666222585e-5
allele num: 120098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2105-6T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2083T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-768T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2105-6T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*973-6T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2083T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2012-6T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2083T>G
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25691
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1844
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41559
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
hgvs: c.2105-6T>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

9-136307737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307737
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307737
    reference: chr 9
allele count: 3
allele frequency: 2.498376055563883e-5
allele num: 120078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2091C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2014C>T
  hgvsp: ENST00000356589.2:c.2014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2107C>T
  hgvsp: ENST00000355699.2:c.2107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2091C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*975C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2107C>T
  hgvsp: ENST00000371929.3:c.2107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2091C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-760C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 7.75e1
  variant carriers: 0
hgvs: c.2107C>T
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

9-136307741-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307741
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307741
    reference: chr 9
allele count: 2
allele frequency: 1.665972511453561e-5
allele num: 120050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2111G>A
  hgvsp: ENSP00000347927.2:p.Arg704His
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2095G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2018G>A
  hgvsp: ENSP00000348997.2:p.Arg673His
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*979G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2095G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2095G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-756G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2111G>A
  hgvsp: ENSP00000360997.3:p.Arg704His
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg704His
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD

9-136307745-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307745
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307745
    reference: chr 9
allele count: 1
allele frequency: 8.330417687142833e-6
allele num: 120042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-752G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2099G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2115G>A
  hgvsp: ENSP00000360997.3:p.Trp705Ter
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2099G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2115G>A
  hgvsp: ENSP00000347927.2:p.Trp705Ter
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*983G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2022G>A
  hgvsp: ENSP00000348997.2:p.Trp674Ter
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2099G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Trp705Ter
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

9-136307764-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307764
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307764
    reference: chr 9
allele count: 1
allele frequency: 8.337641114575865e-6
allele num: 119938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-733G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2118G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2041G>C
  hgvsp: ENSP00000348997.2:p.Asp681His
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2118G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2134G>C
  hgvsp: ENSP00000360997.3:p.Asp712His
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2134G>C
  hgvsp: ENSP00000347927.2:p.Asp712His
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1002G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2118G>C
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10819
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1664
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp712His
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/9-136307766-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307766
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307766
    reference: chr 9
allele count: 1
allele frequency: 8.3380582329987e-6
allele num: 119932
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2136C>A
  hgvsp: ENSP00000360997.3:p.Asp712Glu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2120C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-731C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2043C>A
  hgvsp: ENSP00000348997.2:p.Asp681Glu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2136C>A
  hgvsp: ENSP00000347927.2:p.Asp712Glu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1004C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2120C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2120C>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp712Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

9-136307785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307785
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307785
    reference: chr 9
allele count: 1
allele frequency: 8.351288603831571e-6
allele num: 119742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2062G>A
  hgvsp: ENSP00000348997.2:p.Val688Met
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2155G>A
  hgvsp: ENSP00000347927.2:p.Val719Met
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2139G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2139G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-712G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1023G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2155G>A
  hgvsp: ENSP00000360997.3:p.Val719Met
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2139G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41304
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2123
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val719Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

9-136307794-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307794
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307794
    reference: chr 9
allele count: 1
allele frequency: 8.363581620193032e-6
allele num: 119566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1032G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2071G>C
  hgvsp: ENSP00000348997.2:p.Val691Leu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2148G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-703G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2148G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2164G>C
  hgvsp: ENSP00000360997.3:p.Val722Leu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2164G>C
  hgvsp: ENSP00000347927.2:p.Val722Leu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2148G>C
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41051
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val722Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

http://identifiers.org/exac.variant/9-136307797-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307797
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307797
    reference: chr 9
allele count: 18
allele frequency: 1.506175318807109e-4
allele num: 119508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-700C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2151C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2074C>A
  hgvsp: ENSP00000348997.2:p.Gln692Lys
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2167C>A
  hgvsp: ENSP00000360997.3:p.Gln723Lys
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2151C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2167C>A
  hgvsp: ENSP00000347927.2:p.Gln723Lys
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1035C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2151C>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25185
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41006
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln723Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

9-136307803-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307803
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307803
    reference: chr 9
allele count: 1
allele frequency: 8.383916294979712e-6
allele num: 119276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2157C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2157C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2157C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2080C>G
  hgvsp: ENSP00000348997.2:p.Gln694Glu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-694C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2173C>G
  hgvsp: ENSP00000360997.3:p.Gln725Glu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2173C>G
  hgvsp: ENSP00000347927.2:p.Gln725Glu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1041C>G
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10560
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln725Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

9-136307807-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307807
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307807
    reference: chr 9
allele count: 1
allele frequency: 8.381808123648433e-6
allele num: 119306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1045G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1252+2161G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-690G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1236+2161G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.984+2161G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2177G>A
  hgvsp: ENSP00000360997.3:p.Gly726Glu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2084G>A
  hgvsp: ENSP00000348997.2:p.Gly695Glu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2177G>A
  hgvsp: ENSP00000347927.2:p.Gly726Glu
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10587
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly726Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

9-136307821-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307821
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307821
    reference: chr 9
allele count: 1
allele frequency: 8.401384548173538e-6
allele num: 119028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2098C>T
  hgvsp: ENSP00000348997.2:p.Pro700Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2191C>T
  hgvsp: ENSP00000347927.2:p.Pro731Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-676C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2191C>T
  hgvsp: ENSP00000360997.3:p.Pro731Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2163C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1059C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2163C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2163C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41038
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro731Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

9-136307825-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307825
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307825
    reference: chr 9
allele count: 1224
allele frequency: 1.028156709898528e-2
allele num: 119048
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2195C>T
  hgvsp: ENSP00000360997.3:p.Ala732Val
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2195C>T
  hgvsp: ENSP00000347927.2:p.Ala732Val
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2159C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1063C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2159C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2102C>T
  hgvsp: ENSP00000348997.2:p.Ala701Val
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2159C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-672C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 25266
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 4.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 337
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 20761
  bin: 3.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41234
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala732Val
num of homozygotes: 11
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

9-136307826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307826
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307826
    reference: chr 9
allele count: 5
allele frequency: 4.202316316753795e-5
allele num: 118982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2103G>A
  hgvsp: ENST00000356589.2:c.2103G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2196G>A
  hgvsp: ENST00000355699.2:c.2196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2158G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1064G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2158G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-671G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2196G>A
  hgvsp: ENST00000371929.3:c.2196G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2158G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10722
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2112
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala732Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-136307830-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307830
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307830
    reference: chr 9
allele count: 1
allele frequency: 8.409580193756727e-6
allele num: 118912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2107C>A
  hgvsp: ENSP00000348997.2:p.Pro703Thr
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2154C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2154C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-667C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2154C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2200C>A
  hgvsp: ENSP00000347927.2:p.Pro734Thr
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2200C>A
  hgvsp: ENSP00000360997.3:p.Pro734Thr
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1068C>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro734Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ

9-136307841-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307841
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307841
    reference: chr 9
allele count: 2
allele frequency: 1.684380737421887e-5
allele num: 118738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2143C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1079C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2118C>T
  hgvsp: ENST00000356589.2:c.2118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2211C>T
  hgvsp: ENST00000371929.3:c.2211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2143C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2211C>T
  hgvsp: ENST00000355699.2:c.2211C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-656C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2143C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys737Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

9-136307844-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307844
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307844
    reference: chr 9
allele count: 16
allele frequency: 1.348049540820625e-4
allele num: 118690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2121G>C
  hgvsp: ENST00000356589.2:c.2121G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-653G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2214G>C
  hgvsp: ENST00000371929.3:c.2214G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2214G>C
  hgvsp: ENST00000355699.2:c.2214G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2140G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2140G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2140G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1082G>C
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21085
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25594
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42149
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 9.75e1
  variant carriers: 16
hgvs: p.Val738Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

9-136307846-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307846
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307846
    reference: chr 9
allele count: 1
allele frequency: 8.428860418071477e-6
allele num: 118640
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2216T>C
  hgvsp: ENSP00000360997.3:p.Leu739Pro
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2123T>C
  hgvsp: ENSP00000348997.2:p.Leu708Pro
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1084T>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2216T>C
  hgvsp: ENSP00000347927.2:p.Leu739Pro
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2138T>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2138T>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2138T>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-651T>C
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4965
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10682
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42049
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2104
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu739Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

9-136307847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307847
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307847
    reference: chr 9
allele count: 83
allele frequency: 6.9986677234936e-4
allele num: 118594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2124C>T
  hgvsp: ENST00000356589.2:c.2124C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1085C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2137C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-650C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2217C>T
  hgvsp: ENST00000371929.3:c.2217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2137C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2137C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2217C>T
  hgvsp: ENST00000355699.2:c.2217C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21064
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 25516
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu739Leu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-136307848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307848
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307848
    reference: chr 9
allele count: 405
allele frequency: 3.415300546448087e-3
allele num: 118584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2136G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1086G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2218G>A
  hgvsp: ENSP00000360997.3:p.Glu740Lys
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2218G>A
  hgvsp: ENSP00000347927.2:p.Glu740Lys
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-649G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2136G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2125G>A
  hgvsp: ENSP00000348997.2:p.Glu709Lys
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2136G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 25526
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 21081
  bin: 3.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42038
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2087
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu740Lys
num of homozygotes: 6
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-136307850-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307850
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307850
    reference: chr 9
allele count: 1
allele frequency: 8.441098018030185e-6
allele num: 118468
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2220A>T
  hgvsp: ENSP00000360997.3:p.Glu740Asp
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2134A>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2220A>T
  hgvsp: ENSP00000347927.2:p.Glu740Asp
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-647A>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2127A>T
  hgvsp: ENSP00000348997.2:p.Glu709Asp
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2134A>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1088A>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2134A>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10719
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu740Asp
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS

9-136307857-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307857
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307857
    reference: chr 9
allele count: 1
allele frequency: 8.463530646444471e-6
allele num: 118154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2127C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2134C>G
  hgvsp: ENSP00000348997.2:p.Pro712Ala
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2227C>G
  hgvsp: ENSP00000360997.3:p.Pro743Ala
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1095C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2127C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-640C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2127C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2227C>G
  hgvsp: ENSP00000347927.2:p.Pro743Ala
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25393
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2062
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro743Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-136307857-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307857
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307857
    reference: chr 9
allele count: 1
allele frequency: 8.463530646444471e-6
allele num: 118154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-640C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2134C>T
  hgvsp: ENSP00000348997.2:p.Pro712Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2227C>T
  hgvsp: ENSP00000360997.3:p.Pro743Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2127C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2127C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2227C>T
  hgvsp: ENSP00000347927.2:p.Pro743Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1095C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2127C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10597
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro743Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

9-136307874-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307874
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307874
    reference: chr 9
allele count: 2
allele frequency: 1.712856702408277e-5
allele num: 116764
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+10G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+10G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2110G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2110G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-623G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+10G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2110G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+10G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20284
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

9-136307874-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307874
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307874
    reference: chr 9
allele count: 1
allele frequency: 8.564283512041383e-6
allele num: 116764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-623G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+10G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+10G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2110G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+10G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2110G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+10G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2110G>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9873
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1529
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/9-136307881-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307881
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307881
    reference: chr 9
allele count: 7
allele frequency: 6.080717177157352e-5
allele num: 115118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2103C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-616C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+17C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2103C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+17C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+17C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2103C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+17C>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7910
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17948
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9301
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 8503
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

9-136307884-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307884
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307884
    reference: chr 9
allele count: 7
allele frequency: 6.11332355201565e-5
allele num: 114504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+20C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+20C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2100C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+20C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2100C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-613C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+20C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2100C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16868
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32652
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

9-136307885-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307885
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307885
    reference: chr 9
allele count: 2
allele frequency: 1.75284837861525e-5
allele num: 114100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+21G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2099G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+21G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+21G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-612G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2099G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+21G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2099G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12628
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

9-136307886-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307886
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307886
    reference: chr 9
allele count: 1
allele frequency: 8.760709967935801e-6
allele num: 114146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+22C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-611C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2098C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+22C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+22C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2098C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2098C>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+22C>G
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7703
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/9-136307891-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307891
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307891
    reference: chr 9
allele count: 1
allele frequency: 8.865719807791194e-6
allele num: 112794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+27C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2093C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+27C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-606C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+27C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2093C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+27C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2093C>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2308
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3021
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17544
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-136307892-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307892
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307891
    reference: chr 9
allele count: 1
allele frequency: 8.888888888888888e-6
allele num: 112500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2090delA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+30delA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2090delA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2090delA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+30delA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+30delA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+30delA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-603delA
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23113
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18620
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: CA
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

9-136307892-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307892
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307892
    reference: chr 9
allele count: 1
allele frequency: 8.888888888888888e-6
allele num: 112500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+28C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2092C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2092C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-605C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+28C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+28C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2092C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+28C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23113
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2582
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6673
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

9-136307895-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307895
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307895
    reference: chr 9
allele count: 1
allele frequency: 9.071446714322e-6
allele num: 110236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+31G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+31G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2089G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-602G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2089G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+31G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+31G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2089G>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8758
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4935
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3651
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16847
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

9-136307897-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307897
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307897
    reference: chr 9
allele count: 2
allele frequency: 1.812710727622086e-5
allele num: 110332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+33G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2087G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+33G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-600G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2087G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+33G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2087G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+33G>C
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8578
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9947
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

9-136307900-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307900
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307900
    reference: chr 9
allele count: 6
allele frequency: 5.505496320493293e-5
allele num: 108982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2084A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2084A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+36A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+36A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+36A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-597A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+36A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2084A>G
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12632
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22313
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5720
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

9-136307904-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307904
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307904
    reference: chr 9
allele count: 1
allele frequency: 9.601905017955563e-6
allele num: 104146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2080A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2080A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+40A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+40A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+40A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-593A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2080A>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+40A>G
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17875
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5814
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25000
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2438
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7564
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

9-136307905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307905
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307905
    reference: chr 9
allele count: 4
allele frequency: 4.148516905206389e-5
allele num: 96420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2079G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+41G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2079G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+41G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2079G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+41G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+41G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-592G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18063
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8519
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3903
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4276
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

9-136307909-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307909
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307909
    reference: chr 9
allele count: 1
allele frequency: 1.045696957021855e-5
allele num: 95630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2075T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+45T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2075T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+45T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+45T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2075T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+45T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-588T>G
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17437
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22370
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5390
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3762
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8485
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4492
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

9-136307910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307910
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307910
    reference: chr 9
allele count: 2
allele frequency: 2.130969377970039e-5
allele num: 93854
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-587C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2074C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+46C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+46C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+46C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2074C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+46C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2074C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20184
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6786
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8538
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2323
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

9-136307911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307911
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307911
    reference: chr 9
allele count: 4
allele frequency: 4.423115200035385e-5
allele num: 90434
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-586C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2073C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+47C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2073C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2073C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+47C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+47C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+47C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16670
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6345
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19758
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19967
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4886
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5816
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6682
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1435
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

9-136307912-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136307912
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136307912
    reference: chr 9
allele count: 16
allele frequency: 2.125116217293133e-4
allele num: 75290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-2072G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1102+48G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-2072G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2234+48G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-585G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-2072G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2234+48G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2141+48G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14651
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12703
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20027
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5452
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5944
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9088
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

9-136308447-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308447
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308447
    reference: chr 9
allele count: 1
allele frequency: 2.257642118571364e-5
allele num: 44294
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2235-50G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-50G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1103-50G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1537G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1537G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2142-50G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2235-50G>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1537G>C
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12742
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4813
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

9-136308454-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308454
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308454
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 44504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-43C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2235-43C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2142-43C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1530C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2235-43C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1530C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1103-43C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1530C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25980
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8970
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4218
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5058
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-136308470-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308470
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308470
    reference: chr 9
allele count: 1
allele frequency: 2.116222965251619e-5
allele num: 47254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1514G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-27G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1103-27G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2142-27G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2235-27G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1514G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1514G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2235-27G>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7463
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4777
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/9-136308474-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308474
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308474
    reference: chr 9
allele count: 2
allele frequency: 4.116073266104137e-5
allele num: 48590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2235-23C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2235-23C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-23C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2142-23C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1510C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1510C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1103-23C>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1510C>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27819
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12060
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

9-136308474-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308474
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308474
    reference: chr 9
allele count: 3
allele frequency: 6.174109899156205e-5
allele num: 48590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1510C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1510C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2142-23C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1103-23C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2235-23C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1510C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2235-23C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-23C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12060
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6205
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26950
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6778
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

9-136308477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308477
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308477
    reference: chr 9
allele count: 3
allele frequency: 5.956872244946587e-5
allele num: 50362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2235-20C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-20C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2235-20C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1507C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1507C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1507C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2142-20C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1103-20C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28008
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11609
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6936
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6106
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

9-136308478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308478
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308478
    reference: chr 9
allele count: 1
allele frequency: 1.961015021375064e-5
allele num: 50994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2235-19G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-19G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1506G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1506G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2142-19G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2235-19G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1506G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1103-19G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5778
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

9-136308489-TTCCTCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308489
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308483
    reference: chr 9
allele count: 1
allele frequency: 1.756666549555563e-5
allele num: 56926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1103-7_*1103-2delTCCTCA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2142-7_2142-2delTCCTCA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2235-7_2235-2delTCCTCA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2235-7_2235-2delTCCTCA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*773-7_*773-2delTCCTCA
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 27059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4336
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 9.25e1
  variant carriers: 0
hgvs: c.2235-7_2235-2delTCCTCA
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: TTCCTCA
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-136308502-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308502
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308502
    reference: chr 9
allele count: 1
allele frequency: 1.575001575001575e-5
allele num: 63492
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2240C>T
  hgvsp: ENSP00000360997.3:p.Ala747Val
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1108C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2147C>T
  hgvsp: ENSP00000348997.2:p.Ala716Val
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1482C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*778C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1482C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2240C>T
  hgvsp: ENSP00000347927.2:p.Ala747Val
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1482C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15754
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15637
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala747Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

9-136308503-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308503
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308503
    reference: chr 9
allele count: 2
allele frequency: 3.110613412965037e-5
allele num: 64296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1481G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1481G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2241G>T
  hgvsp: ENST00000371929.3:c.2241G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1109G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2241G>T
  hgvsp: ENST00000355699.2:c.2241G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*779G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1481G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2148G>T
  hgvsp: ENST00000356589.2:c.2148G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3556
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25247
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala747Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-136308516-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308516
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308516
    reference: chr 9
allele count: 15
allele frequency: 2.186333955223881e-4
allele num: 68608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1468G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2254G>A
  hgvsp: ENSP00000347927.2:p.Gly752Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2161G>A
  hgvsp: ENSP00000348997.2:p.Gly721Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*792G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1468G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1122G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2254G>A
  hgvsp: ENSP00000360997.3:p.Gly752Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1468G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7633
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16062
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22154
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2720
  bin: 3.25e1
  variant carriers: 1
hgvs: p.Gly752Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/9-136308521-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308521
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308521
    reference: chr 9
allele count: 1
allele frequency: 1.42836737608913e-5
allele num: 70010
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1463A>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2259A>C
  hgvsp: ENST00000355699.2:c.2259A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1463A>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1127A>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2259A>C
  hgvsp: ENST00000371929.3:c.2259A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*797A>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2166A>C
  hgvsp: ENST00000356589.2:c.2166A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1463A>C
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16142
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2705
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro753Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

9-136308527-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308527
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308527
    reference: chr 9
allele count: 5
allele frequency: 7.051589428257129e-5
allele num: 70906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1457C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2265C>T
  hgvsp: ENST00000355699.2:c.2265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1457C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2172C>T
  hgvsp: ENST00000356589.2:c.2172C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*803C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1457C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1133C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2265C>T
  hgvsp: ENST00000371929.3:c.2265C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15446
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2743
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2935
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser755Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

9-136308528-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308528
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308528
    reference: chr 9
allele count: 1
allele frequency: 1.404218271688151e-5
allele num: 71214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*804G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2266G>A
  hgvsp: ENSP00000347927.2:p.Ala756Thr
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1134G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1456G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2173G>A
  hgvsp: ENSP00000348997.2:p.Ala725Thr
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1456G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2266G>A
  hgvsp: ENSP00000360997.3:p.Ala756Thr
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1456G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala756Thr
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

9-136308530-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308530
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308530
    reference: chr 9
allele count: 2
allele frequency: 2.781022303798876e-5
allele num: 71916
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2268C>T
  hgvsp: ENST00000371929.3:c.2268C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1454C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2268C>T
  hgvsp: ENST00000355699.2:c.2268C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1454C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2175C>T
  hgvsp: ENST00000356589.2:c.2175C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1136C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*806C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1454C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20509
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15793
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1909
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala756Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

9-136308536-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308536
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308536
    reference: chr 9
allele count: 1
allele frequency: 1.383891502906172e-5
allele num: 72260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1448T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1448T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1142T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1448T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2274T>G
  hgvsp: ENSP00000360997.3:p.Cys758Trp
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*812T>G
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2274T>G
  hgvsp: ENSP00000347927.2:p.Cys758Trp
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2181T>G
  hgvsp: ENSP00000348997.2:p.Cys727Trp
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15044
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20949
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3516
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys758Trp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

9-136308540-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308540
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308540
    reference: chr 9
allele count: 2
allele frequency: 2.770850651149903e-5
allele num: 72180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1146G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*816G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1444G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2185G>A
  hgvsp: ENSP00000348997.2:p.Gly729Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2278G>A
  hgvsp: ENSP00000347927.2:p.Gly760Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1444G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2278G>A
  hgvsp: ENSP00000360997.3:p.Gly760Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1444G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19933
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13939
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1259
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2687
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly760Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-136308542-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308542
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308542
    reference: chr 9
allele count: 44988
allele frequency: 5.124968672392973e-1
allele num: 87782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2280C>T
  hgvsp: ENST00000355699.2:c.2280C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1148C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1442C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1442C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*818C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1442C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2187C>T
  hgvsp: ENST00000356589.2:c.2187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2280C>T
  hgvsp: ENST00000371929.3:c.2280C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.75e1
  variant carriers: 655
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.25e1
  variant carriers: 767
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.25e1
  variant carriers: 529
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 10888
  bin: 2.25e1
  variant carriers: 7024
genotype depth: GenotypeDepth
  all individuals: 5428
  bin: 2.75e1
  variant carriers: 3572
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 3.25e1
  variant carriers: 1777
genotype depth: GenotypeDepth
  all individuals: 11815
  bin: 1.25e1
  variant carriers: 8510
genotype depth: GenotypeDepth
  all individuals: 11447
  bin: 7.5e0
  variant carriers: 3918
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 2.5e0
  variant carriers: 480
genotype depth: GenotypeDepth
  all individuals: 10985
  bin: 1.75e1
  variant carriers: 9515
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 3.75e1
  variant carriers: 1094
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 5.75e1
  variant carriers: 352
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 129
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 2.75e1
  variant carriers: 661
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 8.25e1
  variant carriers: 860
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 4.25e1
  variant carriers: 849
genotype quality: GenotypeQuality
  all individuals: 2074
  bin: 7.5e0
  variant carriers: 345
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 3.25e1
  variant carriers: 1150
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 3.75e1
  variant carriers: 1423
genotype quality: GenotypeQuality
  all individuals: 5657
  bin: 6.25e1
  variant carriers: 1150
hgvs: p.Gly760Gly
num of homozygotes: 10960
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-136308543-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308543
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308543
    reference: chr 9
allele count: 1
allele frequency: 1.353949470605757e-5
allele num: 73858
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1441G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2281G>A
  hgvsp: ENSP00000347927.2:p.Gly761Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2281G>A
  hgvsp: ENSP00000360997.3:p.Gly761Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1441G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*819G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1441G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2188G>A
  hgvsp: ENSP00000348997.2:p.Gly730Ser
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1149G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2326
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24531
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly761Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

9-136308549-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308549
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308549
    reference: chr 9
allele count: 5
allele frequency: 7.19196801012629e-5
allele num: 69522
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2287C>T
  hgvsp: ENSP00000360997.3:p.Arg763Trp
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1435C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1435C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1435C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*825C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2194C>T
  hgvsp: ENSP00000348997.2:p.Arg732Trp
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1155C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2287C>T
  hgvsp: ENSP00000347927.2:p.Arg763Trp
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13940
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5687
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7883
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24913
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4591
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3054
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg763Trp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

9-136308550-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308550
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308550
    reference: chr 9
allele count: 1
allele frequency: 1.432870038687491e-5
allele num: 69790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1434G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1156G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2288G>A
  hgvsp: ENSP00000360997.3:p.Arg763Gln
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*826G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1434G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1434G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2288G>A
  hgvsp: ENSP00000347927.2:p.Arg763Gln
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2195G>A
  hgvsp: ENSP00000348997.2:p.Arg732Gln
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7934
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3035
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg763Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

9-136308550-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308550
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308550
    reference: chr 9
allele count: 1
allele frequency: 1.432870038687491e-5
allele num: 69790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1434G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2288G>T
  hgvsp: ENSP00000360997.3:p.Arg763Leu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*826G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2288G>T
  hgvsp: ENSP00000347927.2:p.Arg763Leu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1156G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1434G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1434G>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2195G>T
  hgvsp: ENSP00000348997.2:p.Arg732Leu
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19851
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13911
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7934
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3425
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11825
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4664
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg763Leu
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

9-136308555-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308555
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308555
    reference: chr 9
allele count: 4
allele frequency: 6.006186371963122e-5
allele num: 66598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1429C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*831C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1429C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2200C>T
  hgvsp: ENSP00000348997.2:p.Arg734Trp
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1161C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1429C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2293C>T
  hgvsp: ENSP00000347927.2:p.Arg765Trp
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2293C>T
  hgvsp: ENSP00000360997.3:p.Arg765Trp
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20814
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13977
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3531
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4882
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25621
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg765Trp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

9-136308564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308564
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308564
    reference: chr 9
allele count: 1
allele frequency: 1.585389054473968e-5
allele num: 63076
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2302C>T
  hgvsp: ENSP00000360997.3:p.Arg768Cys
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2302C>T
  hgvsp: ENSP00000347927.2:p.Arg768Cys
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1420C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1170C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1420C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2209C>T
  hgvsp: ENSP00000348997.2:p.Arg737Cys
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*840C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1420C>T
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3340
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3071
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg768Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

9-136308565-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308565
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308565
    reference: chr 9
allele count: 7
allele frequency: 1.120215081295609e-4
allele num: 62488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1171G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2303G>A
  hgvsp: ENSP00000360997.3:p.Arg768His
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2303G>A
  hgvsp: ENSP00000347927.2:p.Arg768His
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*841G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1419G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1419G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2210G>A
  hgvsp: ENSP00000348997.2:p.Arg737His
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1419G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5270
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13552
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22616
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5395
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg768His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-136308570-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308570
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308570
    reference: chr 9
allele count: 13
allele frequency: 2.116643329317138e-4
allele num: 61418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2215G>A
  hgvsp: ENSP00000348997.2:p.Val739Met
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1414G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2308G>A
  hgvsp: ENSP00000347927.2:p.Val770Met
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*846G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1414G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1414G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2308G>A
  hgvsp: ENSP00000360997.3:p.Val770Met
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1176G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23250
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13329
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5493
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9709
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28327
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val770Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

9-136308600-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308600
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308600
    reference: chr 9
allele count: 2
allele frequency: 3.710988236167291e-5
allele num: 53894
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2338T>C
  hgvsp: ENST00000355699.2:c.2338T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2245T>C
  hgvsp: ENST00000356589.2:c.2245T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1206T>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*876T>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1384T>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1384T>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1384T>C
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2338T>C
  hgvsp: ENST00000371929.3:c.2338T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6578
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9394
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu780Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

9-136308604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308604
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308604
    reference: chr 9
allele count: 1
allele frequency: 1.920049153258323e-5
allele num: 52082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1380C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2249C>T
  hgvsp: ENSP00000348997.2:p.Pro750Leu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1380C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1380C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1210C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2342C>T
  hgvsp: ENSP00000347927.2:p.Pro781Leu
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*880C>T
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2342C>T
  hgvsp: ENSP00000360997.3:p.Pro781Leu
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12323
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31666
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8959
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro781Leu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

9-136308613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308613
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308613
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 48768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1371G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1371G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2258G>A
  hgvsp: ENSP00000348997.2:p.Arg753Gln
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1371G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2351G>A
  hgvsp: ENSP00000360997.3:p.Arg784Gln
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2351G>A
  hgvsp: ENSP00000347927.2:p.Arg784Gln
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*889G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1219G>A
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27231
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8560
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg784Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

9-136308614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 136308614
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 136308614
    reference: chr 9
allele count: 1
allele frequency: 2.065347598000744e-5
allele num: 48418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000347927
  ensembl transcript: ENST00000355699
  gene symbol: ADAMTS13
  hgvsc: ENST00000355699.2:c.2352G>A
  hgvsp: ENST00000355699.2:c.2352G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435305
  ensembl transcript: ENST00000474918
  gene symbol: ADAMTS13
  hgvsc: ENST00000474918.1:c.*890G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000348997
  ensembl transcript: ENST00000356589
  gene symbol: ADAMTS13
  hgvsc: ENST00000356589.2:c.2259G>A
  hgvsp: ENST00000356589.2:c.2259G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360984
  ensembl transcript: ENST00000371916
  gene symbol: ADAMTS13
  hgvsc: ENST00000371916.1:c.*1220G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000435274
  ensembl transcript: ENST00000495234
  gene symbol: ADAMTS13
  hgvsc: ENST00000495234.1:c.*1253-1370G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl transcript: ENST00000485925
  gene symbol: ADAMTS13
  hgvsc: ENST00000485925.1:n.1237-1370G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000444504
  ensembl transcript: ENST00000536611
  gene symbol: ADAMTS13
  hgvsc: ENST00000536611.1:c.985-1370G>A
  variant of: http://identifiers.org/hgnc/1366
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000160323
  ensembl protein: ENSP00000360997
  ensembl transcript: ENST00000371929
  gene symbol: ADAMTS13
  hgvsc: ENST00000371929.3:c.2352G>A
  hgvsp: ENST00000371929.3:c.2352G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1366
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7753
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11990
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg784Arg
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1675
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 10844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 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: 2
allele frequency: 3.044047365377005e-5
allele num: 65702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.839431e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.276e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

FS
type: SiteQuality
SIO_000300: 5.575e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.217000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41676
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10840
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1675
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 3
allele frequency: 2.922267679719462e-4
allele num: 10266
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65682
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.551e0

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

DP
type: SiteQuality
SIO_000300: 1.838873e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 7.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

MQ
type: SiteQuality
SIO_000300: 5.927e1

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 159
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1829
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 8.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.518372304889159e-4
allele num: 6586
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522997258604934e-5
allele num: 65660
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.525e0

VQSLOD
type: SiteQuality
SIO_000300: -8.23e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 1.838572e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.605e0

FS
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 1.445e1

GenotypeQuality
all individuals: 1835
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523229246001523e-5
allele num: 65650
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.252e0

MQRankSum
type: SiteQuality
SIO_000300: -1.258e0

FS
type: SiteQuality
SIO_000300: 2.528e0

QD
type: SiteQuality
SIO_000300: 1.315e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.838348e6

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1822
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.519756838905775e-4
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65574
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

MQ
type: SiteQuality
SIO_000300: 5.911e1

FS
type: SiteQuality
SIO_000300: 3.857e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

DP
type: SiteQuality
SIO_000300: 1.835493e6

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

VQSLOD
type: SiteQuality
SIO_000300: -4.856e-1

QD
type: SiteQuality
SIO_000300: 1.031e1

GenotypeQuality
all individuals: 127
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2132
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1823
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41613
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10813
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52494815176284e-5
allele num: 65576
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.384e1

VQSLOD
type: SiteQuality
SIO_000300: 9.97e-1

FS
type: SiteQuality
SIO_000300: 6.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.172e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 1.835257e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.228e0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1658
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10718
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527510463446675e-5
allele num: 65466
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.384e1

FS
type: SiteQuality
SIO_000300: 5.312e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.95e-1

DP
type: SiteQuality
SIO_000300: 1.829312e6

GenotypeQuality
all individuals: 2119
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1657
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10655
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.83477576711251e-5
allele num: 10168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.61e-2

DP
type: SiteQuality
SIO_000300: 1.825602e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.123e0

QD
type: SiteQuality
SIO_000300: 1.487e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 1.403e0

GenotypeQuality
all individuals: 1657
bin: 9.75e1
variant carriers: 18

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

GenotypeQuality
all individuals: 1810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10644
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65316
num of homozygotes: 0

East Asian
type: Population
allele count: 18
allele frequency: 2.097902097902098e-3
allele num: 8580
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.824668e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.349e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

QD
type: SiteQuality
SIO_000300: 1.157e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.25e-1

GenotypeQuality
all individuals: 1797
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 8.75e1
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GenotypeQuality
all individuals: 40666
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534966537729477e-5
allele num: 65148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 1.820308e6

FS
type: SiteQuality
SIO_000300: 4.987e0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 1.068e1

VQSLOD
type: SiteQuality
SIO_000300: -4.616e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.829e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

GenotypeQuality
all individuals: 249
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

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

GenotypeQuality
all individuals: 610
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variant carriers: 0

GenotypeQuality
all individuals: 2100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40937
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534118802160039e-5
allele num: 65184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.634e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.820252e6

FS
type: SiteQuality
SIO_000300: 1.503e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e0

QD
type: SiteQuality
SIO_000300: 1.307e1

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.61e-1

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

GenotypeQuality
all individuals: 1796
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
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variant carriers: 0

GenotypeQuality
all individuals: 1352
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variant carriers: 0

GenotypeQuality
all individuals: 180
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variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 602
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variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10529
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538650910881339e-5
allele num: 64992
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

FS
type: SiteQuality
SIO_000300: 1.638e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.44e-1

QD
type: SiteQuality
SIO_000300: 1.14e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.89e-1

DP
type: SiteQuality
SIO_000300: 1.818868e6

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

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

GenotypeQuality
all individuals: 152
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 240
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 10514
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variant carriers: 1

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
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variant carriers: 1

GenotypeQuality
all individuals: 1791
bin: 9.75e1
variant carriers: 1208

GenotypeQuality
all individuals: 2078
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variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 82
allele frequency: 1.265041653810552e-2
allele num: 6482
num of homozygotes: 1

South Asian
type: Population
allele count: 40
allele frequency: 2.423361201987156e-3
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 23
allele frequency: 2.279484638255699e-3
allele num: 10090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1013
allele frequency: 1.558365639037598e-2
allele num: 65004
num of homozygotes: 10

Other
type: Population
allele count: 7
allele frequency: 8.009153318077803e-3
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 59
allele frequency: 5.125086865879083e-3
allele num: 11512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.829395e6

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.93e0

QD
type: SiteQuality
SIO_000300: 1.272e1

GenotypeQuality
all individuals: 589
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 153
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 42075
bin: 6.25e1
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GenotypeQuality
all individuals: 240
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variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539266693347289e-5
allele num: 64966
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.423654871546292e-4
allele num: 16504
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 1.47e1

MQRankSum
type: SiteQuality
SIO_000300: 6.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 1.768314e6

FS
type: SiteQuality
SIO_000300: 4.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.676e0

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

GenotypeQuality
all individuals: 237
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 42091
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 584
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variant carriers: 1

GenotypeQuality
all individuals: 1469
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variant carriers: 0

GenotypeQuality
all individuals: 10710
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2113
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540215014015957e-5
allele num: 64926
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.76717e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.243e0

MQRankSum
type: SiteQuality
SIO_000300: 4.68e-1

QD
type: SiteQuality
SIO_000300: 8.32e0

VQSLOD
type: SiteQuality
SIO_000300: 2.11e-1

FS
type: SiteQuality
SIO_000300: 4.49e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 257
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42042
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1790
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2103
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541592156379108e-5
allele num: 64868
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.954210631096954e-5
allele num: 10046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.77e0

VQSLOD
type: SiteQuality
SIO_000300: -4.182e-1

QD
type: SiteQuality
SIO_000300: 1.227e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

FS
type: SiteQuality
SIO_000300: 4.263e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e0

DP
type: SiteQuality
SIO_000300: 1.764061e6

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10679
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
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GenotypeQuality
all individuals: 591
bin: 8.25e1
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GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.127932436659368e-4
allele num: 6394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.850709438618137e-4
allele num: 64840
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212415130940834e-4
allele num: 16496
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.919999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.489e1

FS
type: SiteQuality
SIO_000300: 7.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.05e-1

DP
type: SiteQuality
SIO_000300: 1.763136e6

GenotypeQuality
all individuals: 566
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 93
bin: 5.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 590
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64812
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.427e0

QD
type: SiteQuality
SIO_000300: 9.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.24e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.262e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.199e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

DP
type: SiteQuality
SIO_000300: 1.760757e6

GenotypeQuality
all individuals: 284
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 82

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 7
allele frequency: 6.979062811565304e-4
allele num: 10030
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 75
allele frequency: 1.157586047229511e-3
allele num: 64790
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.759814e6

FS
type: SiteQuality
SIO_000300: 1.589e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 1.289e1

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

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

GenotypeQuality
all individuals: 1714
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10666
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variant carriers: 0

GenotypeQuality
all individuals: 125
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 2

GenotypeQuality
all individuals: 569
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GenotypeQuality
all individuals: 68
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 607
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variant carriers: 397

GenotypeQuality
all individuals: 281
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variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 368
allele frequency: 3.668261562998405e-2
allele num: 10032
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.174364040503828e-5
allele num: 64784
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

Latino
type: Population
allele count: 31
allele frequency: 2.699407871821665e-3
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.157407407407407e-3
allele num: 864
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.092e0

VQSLOD
type: SiteQuality
SIO_000300: 6.76e0

QD
type: SiteQuality
SIO_000300: 1.36e1

DP
type: SiteQuality
SIO_000300: 1.75736e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 135
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 166
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 285
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 2094
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variant carriers: 0

GenotypeQuality
all individuals: 1786
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.000400160064026e-4
allele num: 9996
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64730
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 2.25e0

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

DP
type: SiteQuality
SIO_000300: 1.744176e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: -3.001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.267e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 41934
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549186676994578e-5
allele num: 64550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.33e0

DP
type: SiteQuality
SIO_000300: 1.735099e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.77e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.263e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

GenotypeQuality
all individuals: 546
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 200
bin: 9.75e1
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GenotypeQuality
all individuals: 1731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9954
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170411985018727e-4
allele num: 8544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64550
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.263e-1

QD
type: SiteQuality
SIO_000300: 8.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.735099e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 187
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.134796238244514e-5
allele num: 63800
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.682435e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.075e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.482e0

FS
type: SiteQuality
SIO_000300: 9.246e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-2

QD
type: SiteQuality
SIO_000300: 1.223e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.34e-2

GenotypeQuality
all individuals: 497
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
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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: 62
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 40032
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.137981831573779e-5
allele num: 16292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.223e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.34e-2

FS
type: SiteQuality
SIO_000300: 9.246e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.075e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.482e0

DP
type: SiteQuality
SIO_000300: 1.682435e6

GenotypeQuality
all individuals: 740
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 80
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GenotypeQuality
all individuals: 232
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GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 355
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GenotypeQuality
all individuals: 1369
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GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16128
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.158004158004158e-4
allele num: 9620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.783803068141277e-4
allele num: 11212
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6088
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5904825524064e-5
allele num: 62874
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.822e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

DP
type: SiteQuality
SIO_000300: 1.569079e6

BaseQRankSum
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SIO_000300: -3.266e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 365
bin: 8.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.219679064560268e-5
allele num: 16078
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6046
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.592019439826065e-5
allele num: 62552
num of homozygotes: 1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e0

FS
type: SiteQuality
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QD
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SIO_000300: 1.479e1

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: 4.34e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.525125e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

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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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.604466835670507e-5
allele num: 62326
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16040
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African
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allele count: 1
allele frequency: 1.05241001894338e-4
allele num: 9502
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6018
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

DP
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InbreedingCoeff
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SIO_000300: -3.2e-3

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-1

VQSLOD
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FS
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.222e0

MQRankSum
type: SiteQuality
SIO_000300: 8.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16044
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9508
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.603437770580124e-5
allele num: 62366
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

FS
type: SiteQuality
SIO_000300: 6.307e0

MQRankSum
type: SiteQuality
SIO_000300: -8.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.49e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.926e0

QD
type: SiteQuality
SIO_000300: 1.599e1

VQSLOD
type: SiteQuality
SIO_000300: -1.15e-2

DP
type: SiteQuality
SIO_000300: 1.484051e6

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.622639060167456e-5
allele num: 61628
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

DP
type: SiteQuality
SIO_000300: 1.362816e6

VQSLOD
type: SiteQuality
SIO_000300: -3.524e0

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.586e0

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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.626703972411101e-5
allele num: 61474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

DP
type: SiteQuality
SIO_000300: 1.336577e6

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.841e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.008e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.647e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5924
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10888
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South Asian
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allele frequency: 0.0e0
allele num: 15894
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
allele count: 0
allele frequency: 0.0e0
allele num: 9310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.626703972411101e-5
allele num: 61474
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
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MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.336577e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5748
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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60158
num of homozygotes: 0

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

Latino
type: Population
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allele frequency: 9.380863039399625e-5
allele num: 10660
num of homozygotes: 0

African
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South Asian
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
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DP
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MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.453e0

BaseQRankSum
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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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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Other
type: Population
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East Asian
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South Asian
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Latino
type: Population
allele count: 2
allele frequency: 1.869857890800299e-4
allele num: 10696
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 7.79e-1

MQ
type: SiteQuality
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FS
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QD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
type: Population
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Latino
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East Asian
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allele frequency: 7.573844988639232e-4
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European (Non-Finnish)
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European (Finnish)
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South Asian
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

QD
type: SiteQuality
SIO_000300: 1.504e1

DP
type: SiteQuality
SIO_000300: 1.112451e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

GenotypeQuality
all individuals: 435
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 143
bin: 8.25e1
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GenotypeQuality
all individuals: 7188
bin: 6.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.755987918803119e-5
allele num: 56948
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9922
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5500
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.97275e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

QD
type: SiteQuality
SIO_000300: 9.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.684e0

FS
type: SiteQuality
SIO_000300: 3.274e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.47e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

GenotypeQuality
all individuals: 5066
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2116
bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 6845
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variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 7.984031936127744e-4
allele num: 5010
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52858
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

QD
type: SiteQuality
SIO_000300: 1.309e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.26e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

DP
type: SiteQuality
SIO_000300: 9.23612e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.87e-1

GenotypeQuality
all individuals: 2024
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.25e1
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GenotypeQuality
all individuals: 6823
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 931
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GenotypeQuality
all individuals: 2384
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4948
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.015574575557738e-5
allele num: 14254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6710
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-2

DP
type: SiteQuality
SIO_000300: 9.07544e5

BaseQRankSum
type: SiteQuality
SIO_000300: 8.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.389e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.105e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
all individuals: 1305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.25e1
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GenotypeQuality
all individuals: 4660
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 3195
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 236
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variant carriers: 0

GenotypeQuality
all individuals: 2674
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51584
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.301495972382048e-4
allele num: 8690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4876
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14028
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.84e-1

FS
type: SiteQuality
SIO_000300: 3.123e0

QD
type: SiteQuality
SIO_000300: 1.211e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 8.98607e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

GenotypeQuality
all individuals: 329
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 752
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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: 867
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 130
bin: 9.75e1
variant carriers: 4

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8236
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.460920379839299e-4
allele num: 13690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.398992725237829e-4
allele num: 7148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.007064868336545e-5
allele num: 49824
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.54e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.85019e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 9.02e0

GenotypeQuality
all individuals: 7771
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 132
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GenotypeQuality
all individuals: 33
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 139
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variant carriers: 13

GenotypeQuality
all individuals: 290
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5824
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 1.157216068771698e-3
allele num: 12098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3844
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.066115702479339e-4
allele num: 4840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.394521335185097e-5
allele num: 41762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

FS
type: SiteQuality
SIO_000300: 1.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

DP
type: SiteQuality
SIO_000300: 8.4925e5

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2711
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 369
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variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.646903123345686e-4
allele num: 3778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3134
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2876
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.001e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

DP
type: SiteQuality
SIO_000300: 6.21595e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.34e-2

QD
type: SiteQuality
SIO_000300: 9.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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
all individuals: 1260
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 172
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variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3170
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2926
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9642
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.54e-1

DP
type: SiteQuality
SIO_000300: 6.31905e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.21e-2

QD
type: SiteQuality
SIO_000300: 1.55e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 9.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4234
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variant carriers: 0

GenotypeQuality
all individuals: 25850
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2348
bin: 3.75e1
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GenotypeQuality
all individuals: 4873
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GenotypeQuality
all individuals: 533
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GenotypeQuality
all individuals: 607
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GenotypeQuality
all individuals: 934
bin: 6.75e1
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GenotypeQuality
all individuals: 359
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GenotypeQuality
all individuals: 460
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variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.502502502502502e-4
allele num: 3996
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3522
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.78e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.359e0

VQSLOD
type: SiteQuality
SIO_000300: -2.549e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

DP
type: SiteQuality
SIO_000300: 6.78553e5

QD
type: SiteQuality
SIO_000300: 4.84e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 1258
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.891050583657588e-5
allele num: 25700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1508
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.981514609421586e-4
allele num: 3354
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.512e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

FS
type: SiteQuality
SIO_000300: 3.796e0

QD
type: SiteQuality
SIO_000300: 3.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.479e0

DP
type: SiteQuality
SIO_000300: 7.04399e5

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 464
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3660
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.440214738897023e-4
allele num: 4098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1508
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 5.963029218843172e-4
allele num: 3354
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.479e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.512e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.66e-2

FS
type: SiteQuality
SIO_000300: 3.796e0

DP
type: SiteQuality
SIO_000300: 7.04399e5

QD
type: SiteQuality
SIO_000300: 3.29e0

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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variant carriers: 0

GenotypeQuality
all individuals: 486
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variant carriers: 0

GenotypeQuality
all individuals: 491
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3856
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.777777777777778e-3
allele num: 360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10056
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.74419649543208e-5
allele num: 26708
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 2.834467120181406e-4
allele num: 3528
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.22254e5

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.51e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

QD
type: SiteQuality
SIO_000300: 1.107e1

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
all individuals: 27990
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.687043728338618e-5
allele num: 27122
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.47e-2

DP
type: SiteQuality
SIO_000300: 7.33825e5

VQSLOD
type: SiteQuality
SIO_000300: -1.254e0

FS
type: SiteQuality
SIO_000300: 1.822e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

GenotypeQuality
all individuals: 183
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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
all individuals: 412
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30776
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.154243860404998e-4
allele num: 4642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4676
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.485e0

DP
type: SiteQuality
SIO_000300: 8.07701e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.14e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.096e-1

QD
type: SiteQuality
SIO_000300: 2.57e0

MQ
type: SiteQuality
SIO_000300: 5.303e1

MQRankSum
type: SiteQuality
SIO_000300: -2.899e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.25e-1

GenotypeQuality
all individuals: 277
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variant carriers: 0

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

GenotypeQuality
all individuals: 1262
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variant carriers: 1

GenotypeQuality
all individuals: 2812
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.884005306569764e-5
allele num: 34674
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.74087e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.237e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

FS
type: SiteQuality
SIO_000300: 7.339e0

MQ
type: SiteQuality
SIO_000300: 5.829e1

QD
type: SiteQuality
SIO_000300: 7.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.787e0

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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bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10952
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5152
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.68569479190357e-5
allele num: 35176
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.94e-1

FS
type: SiteQuality
SIO_000300: 9.72e-1

DP
type: SiteQuality
SIO_000300: 8.80507e5

QD
type: SiteQuality
SIO_000300: 2.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-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: 0

GenotypeQuality
all individuals: 1276
bin: 9.75e1
variant carriers: 12

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2380
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.869966294128082e-5
allele num: 11274
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 2.564102564102564e-3
allele num: 5460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5138
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.203e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

DP
type: SiteQuality
SIO_000300: 9.0837e5

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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bin: 7.5e0
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.603488674824265e-5
allele num: 38410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.27e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

MQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.899e-1

DP
type: SiteQuality
SIO_000300: 9.15547e5

GenotypeQuality
all individuals: 670
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15630
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2036
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21753
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3590
bin: 7.5e0
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5408
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 7.183908045977011e-4
allele num: 5568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

DP
type: SiteQuality
SIO_000300: 9.23096e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

GenotypeQuality
all individuals: 452
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3566
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15057
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5568
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.841620626151013e-4
allele num: 5430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39132
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.23069e5

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -9.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.19e-1

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

GenotypeQuality
all individuals: 203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 21570
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
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variant carriers: 0

GenotypeQuality
all individuals: 453
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variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5520
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.492537313432836e-4
allele num: 6700
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.532030181799767e-5
allele num: 39494
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.519e0

DP
type: SiteQuality
SIO_000300: 9.26344e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.059e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

FS
type: SiteQuality
SIO_000300: 1.787e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.17e-1

GenotypeQuality
all individuals: 1915
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2786
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3130
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2340
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2056
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1355
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5584
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 1.470588235294118e-4
allele num: 6800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39660
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.444e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.808e0

DP
type: SiteQuality
SIO_000300: 9.29855e5

VQSLOD
type: SiteQuality
SIO_000300: 4.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.094e1

GenotypeQuality
all individuals: 2484
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3494
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20204
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3344
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 317
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2538
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
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variant carriers: 0

GenotypeQuality
all individuals: 10630
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2866
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.056122964910506e-5
allele num: 39556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5540
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.615e1

VQSLOD
type: SiteQuality
SIO_000300: -1.303e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

FS
type: SiteQuality
SIO_000300: 3.009e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

DP
type: SiteQuality
SIO_000300: 9.28883e5

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
all individuals: 603
bin: 9.25e1
variant carriers: 601

GenotypeQuality
all individuals: 1729
bin: 4.75e1
variant carriers: 1469

GenotypeQuality
all individuals: 22964
bin: 9.75e1
variant carriers: 22956

GenotypeQuality
all individuals: 2064
bin: 2.5e0
variant carriers: 172

GenotypeQuality
all individuals: 1648
bin: 5.25e1
variant carriers: 1384

GenotypeQuality
all individuals: 829
bin: 1.25e1
variant carriers: 449

GenotypeQuality
all individuals: 8780
bin: 2.25e1
variant carriers: 937

GenotypeQuality
all individuals: 1532
bin: 6.75e1
variant carriers: 1088

GenotypeQuality
all individuals: 887
bin: 7.75e1
variant carriers: 823

GenotypeQuality
all individuals: 582
bin: 8.75e1
variant carriers: 579

GenotypeQuality
all individuals: 1135
bin: 1.75e1
variant carriers: 691

GenotypeQuality
all individuals: 702
bin: 7.25e1
variant carriers: 617

GenotypeQuality
all individuals: 967
bin: 5.75e1
variant carriers: 816

Latino
type: Population
allele count: 5090
allele frequency: 5.694786305661221e-1
allele num: 8938
num of homozygotes: 1292

East Asian
type: Population
allele count: 6035
allele frequency: 8.188602442333786e-1
allele num: 7370
num of homozygotes: 2447

European (Non-Finnish)
type: Population
allele count: 22413
allele frequency: 4.733674072822506e-1
allele num: 47348
num of homozygotes: 4730

South Asian
type: Population
allele count: 7211
allele frequency: 5.278916544655929e-1
allele num: 13660
num of homozygotes: 1818

African
type: Population
allele count: 2459
allele frequency: 3.838588822978458e-1
allele num: 6406
num of homozygotes: 395

European (Finnish)
type: Population
allele count: 1479
allele frequency: 4.274566473988439e-1
allele num: 3460
num of homozygotes: 216

Other
type: Population
allele count: 301
allele frequency: 5.016666666666667e-1
allele num: 600
num of homozygotes: 62

BaseQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.210000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.084314e6

QD
type: SiteQuality
SIO_000300: 1.838e1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.05e0

FS
type: SiteQuality
SIO_000300: 5.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

GenotypeQuality
all individuals: 2314
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3004
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
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variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 822
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variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 3.25e1
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GenotypeQuality
all individuals: 1067
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 779
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variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40172
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.77367860943597e-4
allele num: 5638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11914
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.122e0

FS
type: SiteQuality
SIO_000300: 3.834e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.91e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 7.5e0

DP
type: SiteQuality
SIO_000300: 8.63444e5

GenotypeQuality
all individuals: 895
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 3465
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10962
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
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variant carriers: 1

GenotypeQuality
all individuals: 562
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.75e1
variant carriers: 3

South Asian
type: Population
allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6706
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.95587143311764e-5
allele num: 37708
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.879699248120301e-4
allele num: 5320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5266
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.29e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.14e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.911e-1

QD
type: SiteQuality
SIO_000300: 7.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.04e-1

DP
type: SiteQuality
SIO_000300: 8.23268e5

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3425
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4664
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1175
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25700
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 11825
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.640752086194148e-5
allele num: 37868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2590
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6754
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.71e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.54e-1

FS
type: SiteQuality
SIO_000300: 2.424e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.46e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.954e-1

DP
type: SiteQuality
SIO_000300: 8.21308e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.612e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 413
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variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.909125620465827e-4
allele num: 5238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6754
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2590
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.954e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.612e0

FS
type: SiteQuality
SIO_000300: 2.424e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 8.21308e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.46e-2

QD
type: SiteQuality
SIO_000300: 7.71e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5136
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.677615137450911e-4
allele num: 11204
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.778549597110308e-5
allele num: 35990
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.31e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

FS
type: SiteQuality
SIO_000300: 3.399e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.13e-1

DP
type: SiteQuality
SIO_000300: 7.90782e5

QD
type: SiteQuality
SIO_000300: 1.151e1

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

South Asian
type: Population
allele count: 1
allele frequency: 9.247272054743851e-5
allele num: 10814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.444e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

DP
type: SiteQuality
SIO_000300: 7.61347e5

VQSLOD
type: SiteQuality
SIO_000300: -4.57e0

QD
type: SiteQuality
SIO_000300: 1.279e1

MQ
type: SiteQuality
SIO_000300: 5.829e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

FS
type: SiteQuality
SIO_000300: 2.614e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

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
all individuals: 38
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variant carriers: 7

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33636
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.274717121127805e-5
allele num: 10782
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.63826998689384e-4
allele num: 6104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4580
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 1.040366208905535e-3
allele num: 4806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2144
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.562e0

VQSLOD
type: SiteQuality
SIO_000300: 5.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.5704e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.142e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 14

GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 9
allele frequency: 1.897933361450865e-3
allele num: 4742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.05070490712168e-5
allele num: 33054
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10648
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.341129301703976e-4
allele num: 5986
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2080
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.50492e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

QD
type: SiteQuality
SIO_000300: 1.076e1

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1808
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4090
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.02757502027575e-4
allele num: 9864
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3794
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.18e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 5.319e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

DP
type: SiteQuality
SIO_000300: 7.03143e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1752
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 3.625815808556925e-5
allele num: 27580
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3596
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.98e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.79e-2

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.91603e5

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-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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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25764
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1626
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.67841e5

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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