8-144642173-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642173
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642173
    reference: chr 8
allele count: 1
allele frequency: 1.421666192777936e-5
allele num: 70340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+34C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+34C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+34C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1091C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+34C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+34C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+34C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+34C>G
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16793
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1989
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4481
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

8-144642178-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642178
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642178
    reference: chr 8
allele count: 108961
allele frequency: 9.846466654617748e-1
allele num: 110660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+39T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+39T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+39T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+39T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1096T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+39T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+39T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+39T>C
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 3.25e1
  variant carriers: 3405
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.75e1
  variant carriers: 429
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 3.75e1
  variant carriers: 1558
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 838
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 238
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 2.75e1
  variant carriers: 6765
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.75e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 16546
  bin: 1.75e1
  variant carriers: 16511
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 7.5e0
  variant carriers: 4085
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 2.5e0
  variant carriers: 531
genotype depth: GenotypeDepth
  all individuals: 12221
  bin: 1.25e1
  variant carriers: 12118
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 12516
  bin: 2.25e1
  variant carriers: 12494
genotype quality: GenotypeQuality
  all individuals: 3245
  bin: 5.75e1
  variant carriers: 3245
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 3691
  bin: 3.25e1
  variant carriers: 3687
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 1.75e1
  variant carriers: 863
genotype quality: GenotypeQuality
  all individuals: 5100
  bin: 3.75e1
  variant carriers: 5100
genotype quality: GenotypeQuality
  all individuals: 1932
  bin: 2.25e1
  variant carriers: 1826
genotype quality: GenotypeQuality
  all individuals: 6415
  bin: 4.75e1
  variant carriers: 6415
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 1.25e1
  variant carriers: 287
num of homozygotes: 53780
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

8-144642194-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642194
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642194
    reference: chr 8
allele count: 2
allele frequency: 3.987081854790479e-5
allele num: 50162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+55G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+55G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+55G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+55G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+55G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1112G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+55G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+55G>C
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7505
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16809
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12652
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4580
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-144642196-T-TTTTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642196
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642200
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 38352
alternate allele: TTTTA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+74_410+77dupTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+74_410+77dupTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1131_1134dupTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+74_752+77dupTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+74_458+77dupTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+74_410+77dupTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+74_410+77dupTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+74_554+77dupTTTA
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17465
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2984
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12342
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

8-144642196-TTTTA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642196
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642192
    reference: chr 8
allele count: 11
allele frequency: 2.86816854401335e-4
allele num: 38352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+74_458+77delTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1131_1134delTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+74_752+77delTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+74_410+77delTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+74_410+77delTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+74_410+77delTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+74_410+77delTTTA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+74_554+77delTTTA
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13146
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3036
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2112
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: TTTTA
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

8-144642201-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642201
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642201
    reference: chr 8
allele count: 2
allele frequency: 1.022285831118381e-4
allele num: 19564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1119T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+62T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+62T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+62T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+62T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+62T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+62T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+62T>C
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24658
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5009
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5979
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 871
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD

8-144642203-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642203
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642203
    reference: chr 8
allele count: 1
allele frequency: 5.020584396023697e-5
allele num: 19918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1121T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+64T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+64T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+64T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+64T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+64T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+64T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+64T>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25336
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6249
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

8-144642213-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642213
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642213
    reference: chr 8
allele count: 2
allele frequency: 1.460493646852636e-4
allele num: 13694
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+74T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+74T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+74T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+74T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+74T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.4T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1131T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+74T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+74T>G
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3324
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

8-144642218-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642218
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642218
    reference: chr 8
allele count: 2
allele frequency: 1.498351813005694e-4
allele num: 13348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1136A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+79A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+79A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+79A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+79A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.9A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+79A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+79A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+79A>G
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25180
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

8-144642227-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642227
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642226
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 12548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+89delG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+89delG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+89delG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1146delG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+89delG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+89delG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+89delG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.19delG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+89delG
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20427
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: TG
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

8-144642240-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642240
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642240
    reference: chr 8
allele count: 32
allele frequency: 2.608837436817218e-3
allele num: 12266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1158T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+101T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+101T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+101T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+101T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.31T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+101T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+101T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+101T>C
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 7.5e0
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15130
  bin: 2.5e0
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13767
  bin: 7.5e0
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 2.25e1
  variant carriers: 5
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: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

8-144642244-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642244
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642244
    reference: chr 8
allele count: 2791
allele frequency: 2.256994986252628e-1
allele num: 12366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.35A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+105A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+105A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1162A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+105A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+105A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+105A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+105A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+105A>G
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.75e1
  variant carriers: 361
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 390
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 3.25e1
  variant carriers: 388
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 2.25e1
  variant carriers: 213
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 7.5e0
  variant carriers: 569
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11954
  bin: 2.5e0
  variant carriers: 799
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 304
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2730
  bin: 6.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 6.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 1.25e1
  variant carriers: 161
genotype quality: GenotypeQuality
  all individuals: 9593
  bin: 7.5e0
  variant carriers: 438
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 2.25e1
  variant carriers: 152
genotype quality: GenotypeQuality
  all individuals: 2394
  bin: 2.5e0
  variant carriers: 4
num of homozygotes: 330
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP

8-144642249-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642249
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642249
    reference: chr 8
allele count: 1
allele frequency: 8.160600620205648e-5
allele num: 12254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.40G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+110G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+110G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1167G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+110G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+110G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+110G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+110G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+110G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13089
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-144642253-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642253
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642253
    reference: chr 8
allele count: 1
allele frequency: 8.159268929503917e-5
allele num: 12256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+114A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+114A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1171A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+114A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+114A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.44A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+114A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+114A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+114A>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  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: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11551
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

8-144642268-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642268
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642268
    reference: chr 8
allele count: 6
allele frequency: 4.900359359686377e-4
allele num: 12244
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+129T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+129T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+129T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+129T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+129T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+129T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.59T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1186T>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+129T>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9610
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  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: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4033
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8618
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

8-144642281-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642281
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642281
    reference: chr 8
allele count: 215
allele frequency: 1.757684761281884e-2
allele num: 12232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+142C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+142C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+142C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1199C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+142C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.72C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+142C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+142C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+142C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 7587
  bin: 2.5e0
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.5e0
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3811
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.25e1
  variant carriers: 3
num of homozygotes: 3
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD

8-144642290-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642290
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642290
    reference: chr 8
allele count: 2
allele frequency: 1.632386549134835e-4
allele num: 12252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+151T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+151T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+151T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.81T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+151T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+151T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+151T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1208T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+151T>G
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

8-144642299-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642299
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642299
    reference: chr 8
allele count: 1
allele frequency: 8.13140348024069e-5
allele num: 12298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.90C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+160C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1217C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+160C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+160C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+160C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+160C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+160C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+160C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  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: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

8-144642306-AGTGCTGGGATTACAGGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642306
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642289
    reference: chr 8
allele count: 1
allele frequency: 8.107669855683477e-5
allele num: 12334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  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: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4570
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: AGTGCTGGGATTACAGGG
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

8-144642309-G-GAGCCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642309
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642314
    reference: chr 8
allele count: 3
allele frequency: 2.4330900243309e-4
allele num: 12330
alternate allele: GAGCCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+170_410+171insAGCCA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+170_554+171insAGCCA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.100_101insAGCCA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+170_410+171insAGCCA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+170_410+171insAGCCA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+170_752+171insAGCCA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1227_1228insAGCCA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+170_410+171insAGCCA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+170_458+171insAGCCA
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-144642312-GGGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642312
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642309
    reference: chr 8
allele count: 3
allele frequency: 2.43427458617332e-4
allele num: 12324
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+174_410+176delGGA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+174_410+176delGGA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+174_752+176delGGA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+174_458+176delGGA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.104_106delGGA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1231_1233delGGA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+174_410+176delGGA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+174_554+176delGGA
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+174_410+176delGGA
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  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: 2726
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3949
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: GGGA
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

8-144642317-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642317
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642317
    reference: chr 8
allele count: 3
allele frequency: 2.435855797336798e-4
allele num: 12316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+178T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+178T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1235T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+178T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.108T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+178T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+178T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+178T>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+178T>G
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  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: 80
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4469
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-144642318-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642318
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642318
    reference: chr 8
allele count: 3
allele frequency: 2.43427458617332e-4
allele num: 12324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1236A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+179A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+179A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+179A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+179A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+179A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+179A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.109A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+179A>C
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
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: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  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: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

8-144642408-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642408
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642408
    reference: chr 8
allele count: 1
allele frequency: 8.115565654926148e-5
allele num: 12322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.199G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+269G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+269G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1326G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+269G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+269G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+269G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+269G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+269G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
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: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

8-144642416-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642416
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642416
    reference: chr 8
allele count: 1
allele frequency: 8.124796880077999e-5
allele num: 12308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+277C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+277C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+277C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+277C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1334C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+277C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.207C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+277C>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+277C>G
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3299
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

8-144642416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642416
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642416
    reference: chr 8
allele count: 1
allele frequency: 8.124796880077999e-5
allele num: 12308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+277C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+277C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+277C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+277C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.207C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+277C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1334C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+277C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+277C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  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: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4968
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

8-144642431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642431
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642431
    reference: chr 8
allele count: 1
allele frequency: 8.164598301763554e-5
allele num: 12248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+292G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+292G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+292G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+292G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.222G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+292G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1349G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+292G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+292G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  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 quality: GenotypeQuality
  all individuals: 138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

8-144642437-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642437
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642437
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 12166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.458+298A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.410+298A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.410+298A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.410+298A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.228A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.554+298A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1355A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.410+298A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.752+298A>G
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3293
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4762
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

8-144642490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642490
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642490
    reference: chr 8
allele count: 2561
allele frequency: 2.66548709408826e-1
allele num: 9608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-283G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-283G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-283G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-283G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1408G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-283G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-283G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.281G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-283G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 2.25e1
  variant carriers: 473
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 7.5e0
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 1.25e1
  variant carriers: 536
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 2.75e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 2.5e0
  variant carriers: 119
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.75e1
  variant carriers: 712
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 2.25e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 61
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 42
num of homozygotes: 307
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

8-144642535-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642535
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642535
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 3482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-238C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-238C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.326C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-238C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-238C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-238C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1453C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-238C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-238C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 7.5e0
  variant carriers: 1
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: 5659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5354
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

8-144642536-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642536
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642536
    reference: chr 8
allele count: 1
allele frequency: 3.037667071688943e-4
allele num: 3292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-237G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-237G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1454G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-237G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-237G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-237G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.327G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-237G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-237G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-144642557-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642557
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642557
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 1932
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-216G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-216G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-216G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-216G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-216G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1475G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.348G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-216G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-216G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6952
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-144642566-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642566
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642566
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 1742
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-207G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-207G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-207G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-207G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1484G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-207G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.357G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-207G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-207G>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7765
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/8-144642591-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642591
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642591
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 1618
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-182A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-182A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-182A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-182A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-182A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1509A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.382A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-182A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-182A>C
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9862
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  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: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD

8-144642596-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642596
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642596
    reference: chr 8
allele count: 1043
allele frequency: 6.078088578088578e-1
allele num: 1716
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.387T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-177T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-177T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-177T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1514T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-177T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-177T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-177T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-177T>C
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.75e1
  variant carriers: 140
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: 11
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 3.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 7.5e0
  variant carriers: 1278
genotype depth: GenotypeDepth
  all individuals: 5502
  bin: 2.5e0
  variant carriers: 1829
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.25e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 2.5e0
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 8.25e1
  variant carriers: 80
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 75
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 1.25e1
  variant carriers: 590
num of homozygotes: 306
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-144642617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642617
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642617
    reference: chr 8
allele count: 3
allele frequency: 1.849568434032059e-3
allele num: 1622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-156G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-156G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-156G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.408G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-156G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-156G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-156G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-156G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1535G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14898
  bin: 2.5e0
  variant carriers: 6
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: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

8-144642626-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642626
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642626
    reference: chr 8
allele count: 1798
allele frequency: 9.868276619099891e-1
allele num: 1822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-147A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-147A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-147A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-147A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-147A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1544A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-147A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-147A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.417A>G
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 7.5e0
  variant carriers: 1857
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 288
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 2.5e0
  variant carriers: 6372
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 2
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: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 252
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.25e1
  variant carriers: 206
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 1.75e1
  variant carriers: 1400
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 6.75e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.75e1
  variant carriers: 117
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 1.25e1
  variant carriers: 1973
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 8.75e1
  variant carriers: 9
num of homozygotes: 887
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

8-144642629-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642629
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642629
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 1282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.420C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-144C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-144C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-144C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-144C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1547C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-144C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-144C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-144C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 16937
  bin: 2.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16249
  bin: 7.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD

8-144642642-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642642
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642642
    reference: chr 8
allele count: 1
allele frequency: 8.928571428571428e-4
allele num: 1120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.433G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-131G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-131G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-131G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1560G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-131G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-131G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-131G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-131G>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21067
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 1
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: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

8-144642649-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642649
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642649
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 1078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1567C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-124C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.440C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-124C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-124C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-124C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-124C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-124C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-124C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24290
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2062
  bin: 2.5e0
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

8-144642650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642650
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642650
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 1078
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-123G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-123G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-123G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-123G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.441G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1568G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-123G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-123G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-123G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24643
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21846
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/8-144642653-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642653
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642653
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 1076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-120A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-120A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1571A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.444A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-120A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-120A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-120A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-120A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-120A>C
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26807
  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: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.25e1
  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 quality: GenotypeQuality
  all individuals: 1108
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24258
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

8-144642693-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642693
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642693
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 1594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-80C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-80C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1611C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-80C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-80C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.484C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-80C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-80C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-80C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5907
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

8-144642694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642694
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642694
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 1682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-79G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-79G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1612G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.485G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-79G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-79G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-79G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-79G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-79G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40804
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4703
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37603
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

8-144642700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642700
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642700
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 2000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-73G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-73G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-73G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.491G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-73G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-73G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1618G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-73G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-73G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8492
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  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 depth: GenotypeDepth
  all individuals: 41316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6952
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

8-144642710-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642710
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642708
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 2640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-62_411-61delAG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-62_411-61delAG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.502_503delAG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-62_411-61delAG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-62_753-61delAG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-62_459-61delAG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-62_411-61delAG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1629_1630delAG
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-62_555-61delAG
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39925
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: CAG
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-144642714-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642714
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642714
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 3082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-59G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-59G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-59G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-59G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1632G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-59G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.505G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-59G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-59G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.25e1
  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 depth: GenotypeDepth
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14760
  bin: 7.5e0
  variant carriers: 1
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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1602
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

8-144642724-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642724
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642724
    reference: chr 8
allele count: 2
allele frequency: 4.873294346978557e-4
allele num: 4104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-49C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-49C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-49C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-49C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.515C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-49C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-49C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1642C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-49C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35051
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19464
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

8-144642725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642725
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642725
    reference: chr 8
allele count: 2
allele frequency: 4.545454545454545e-4
allele num: 4400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-48G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-48G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-48G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-48G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-48G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.516G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1643G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-48G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-48G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34345
  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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  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: 20332
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32538
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 8.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

8-144642731-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642731
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642731
    reference: chr 8
allele count: 1
allele frequency: 1.81422351233672e-4
allele num: 5512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-42A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-42A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.522A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1649A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-42A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-42A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-42A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-42A>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-42A>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30159
  bin: 2.5e0
  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: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 1.25e1
  variant carriers: 1
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: 47
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24856
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

8-144642732-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642732
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642732
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 5776
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-41G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1650G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-41G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-41G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.523G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-41G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-41G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-41G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-41G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29580
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25413
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28362
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD

8-144642737-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642737
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642737
    reference: chr 8
allele count: 1
allele frequency: 1.435956346927053e-4
allele num: 6964
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1655T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.528T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-36T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-36T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-36T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-36T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-36T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-36T>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-36T>C
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.75e1
  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: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26459
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25433
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 2.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-144642739-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642739
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642739
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 7160
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-34C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-34C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-34C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-34C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-34C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.530C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-34C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1657C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-34C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25238
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24252
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25834
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

8-144642740-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642740
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642740
    reference: chr 8
allele count: 1
allele frequency: 1.240694789081886e-4
allele num: 8060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1658G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-33G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.531G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-33G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-33G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-33G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-33G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-33G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-33G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24137
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27285
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2421
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-144642742-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642742
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642742
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 8642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-31C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.533C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-31C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-31C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-31C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-31C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1660C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-31C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-31C>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22900
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  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: 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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31403
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22069
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

8-144642747-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642747
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642747
    reference: chr 8
allele count: 1
allele frequency: 9.527439024390244e-5
allele num: 10496
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1665C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-26C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.538C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-26C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-26C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-26C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-26C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-26C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-26C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31415
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-144642748-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642748
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642748
    reference: chr 8
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-25G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-25G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-25G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-25G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-25G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-25G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.539G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1666G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-25G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18436
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34904
  bin: 7.5e0
  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: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17891
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-144642751-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642751
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642751
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 12654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1669C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-22C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-22C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.542C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-22C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-22C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-22C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-22C>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-22C>A
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36182
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  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: 16704
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16288
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

8-144642762-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642762
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642762
    reference: chr 8
allele count: 5
allele frequency: 2.981159074648223e-4
allele num: 16772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1680C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-11C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-11C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-11C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-11C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-11C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-11C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-11C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.553C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38168
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12845
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  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: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35794
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12656
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

8-144642764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642764
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642764
    reference: chr 8
allele count: 1
allele frequency: 5.771672630728385e-5
allele num: 17326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1682C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-9C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-9C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-9C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-9C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.555C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-9C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-9C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-9C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  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: 0
  bin: 9.75e1
  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 quality: GenotypeQuality
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2498
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

8-144642765-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642765
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642765
    reference: chr 8
allele count: 1
allele frequency: 5.471656817684395e-5
allele num: 18276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.556G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-8G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-8G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-8G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-8G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-8G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1683G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-8G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-8G>A
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.25e1
  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: 4229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38335
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 6.75e1
  variant carriers: 1
hgvs: c.411-8G>A
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

8-144642765-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642765
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642765
    reference: chr 8
allele count: 2
allele frequency: 1.094331363536879e-4
allele num: 18276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1683G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.753-8G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.459-8G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.411-8G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.411-8G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.411-8G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.411-8G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.555-8G>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.556G>C
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
hgvs: c.411-8G>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

8-144642781-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642781
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642781
    reference: chr 8
allele count: 2
allele frequency: 8.048937540244688e-5
allele num: 24848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1699G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.419G>A
  hgvsp: ENSP00000262580.4:p.Arg140Gln
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.563G>A
  hgvsp: ENSP00000433958.1:p.Arg188Gln
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.761G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.419G>A
  hgvsp: ENSP00000437065.1:p.Arg140Gln
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.572G>A
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.467G>A
  hgvsp: ENSP00000436684.1:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.419G>A
  hgvsp: ENSP00000433209.1:p.Arg140Gln
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.419G>A
  hgvsp: ENSP00000434386.1:p.Arg140Gln
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.75e1
  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: 9452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37375
  bin: 7.5e0
  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: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2235
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg140Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

8-144642783-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642783
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642783
    reference: chr 8
allele count: 2
allele frequency: 7.775445144234507e-5
allele num: 25722
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.469C>T
  hgvsp: ENSP00000436684.1:p.Gln157Ter
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.565C>T
  hgvsp: ENSP00000433958.1:p.Gln189Ter
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.421C>T
  hgvsp: ENSP00000262580.4:p.Gln141Ter
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.763C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.421C>T
  hgvsp: ENSP00000437065.1:p.Gln141Ter
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.421C>T
  hgvsp: ENSP00000434386.1:p.Gln141Ter
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.574C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1701C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.421C>T
  hgvsp: ENSP00000433209.1:p.Gln141Ter
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9234
  bin: 2.5e0
  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: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9412
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln141Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/8-144642790-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642790
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642790
    reference: chr 8
allele count: 1
allele frequency: 3.53456807578114e-5
allele num: 28292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.428A>C
  hgvsp: ENSP00000437065.1:p.Glu143Ala
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1708A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.770A>C
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.428A>C
  hgvsp: ENSP00000434386.1:p.Glu143Ala
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.476A>C
  hgvsp: ENSP00000436684.1:p.Glu159Ala
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.428A>C
  hgvsp: ENSP00000433209.1:p.Glu143Ala
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.428A>C
  hgvsp: ENSP00000262580.4:p.Glu143Ala
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.572A>C
  hgvsp: ENSP00000433958.1:p.Glu191Ala
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.581A>C
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  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: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu143Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD

8-144642791-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642791
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642791
    reference: chr 8
allele count: 17
allele frequency: 5.96616831613673e-4
allele num: 28494
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.771A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.477A>G
  hgvsp: ENST00000534018.1:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.429A>G
  hgvsp: ENST00000526406.1:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.429A>G
  hgvsp: ENST00000262580.4:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.573A>G
  hgvsp: ENST00000533063.1:c.573A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1709A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.582A>G
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.429A>G
  hgvsp: ENST00000533348.1:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.429A>G
  hgvsp: ENST00000533888.1:c.429A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36737
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8579
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  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: 6924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 7000
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35184
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu143Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

8-144642800-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642800
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642800
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 29938
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000526469
  gene symbol: GSDMD
  hgvsc: ENST00000526469.1:n.3C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.591C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.486C>T
  hgvsp: ENST00000534018.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.438C>T
  hgvsp: ENST00000533348.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.780C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1718C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.582C>T
  hgvsp: ENST00000533063.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.438C>T
  hgvsp: ENST00000526406.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.438C>T
  hgvsp: ENST00000262580.4:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.438C>T
  hgvsp: ENST00000533888.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
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: 1111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36182
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val146Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

8-144642801-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642801
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642801
    reference: chr 8
allele count: 6
allele frequency: 2.012342366514623e-4
allele num: 29816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.439C>T
  hgvsp: ENST00000533888.1:c.439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.487C>T
  hgvsp: ENST00000534018.1:c.487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.781C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.583C>T
  hgvsp: ENST00000533063.1:c.583C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.439C>T
  hgvsp: ENST00000526406.1:c.439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.439C>T
  hgvsp: ENST00000533348.1:c.439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.439C>T
  hgvsp: ENST00000262580.4:c.439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.592C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1719C>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000526469
  gene symbol: GSDMD
  hgvsc: ENST00000526469.1:n.4C>T
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8483
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu147Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum

8-144642803-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642803
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642803
    reference: chr 8
allele count: 1
allele frequency: 3.278258589037503e-5
allele num: 30504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.585G>T
  hgvsp: ENST00000533063.1:c.585G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.441G>T
  hgvsp: ENST00000526406.1:c.441G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.441G>T
  hgvsp: ENST00000533348.1:c.441G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.783G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.594G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.489G>T
  hgvsp: ENST00000534018.1:c.489G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.441G>T
  hgvsp: ENST00000533888.1:c.441G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.441G>T
  hgvsp: ENST00000262580.4:c.441G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1721G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000526469
  gene symbol: GSDMD
  hgvsc: ENST00000526469.1:n.6G>T
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8382
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu147Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

8-144642812-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 144642812
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 144642812
    reference: chr 8
allele count: 4
allele frequency: 1.2326656394453e-4
allele num: 32450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000524846
  gene symbol: GSDMD
  hgvsc: ENST00000524846.1:n.1730G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000434386
  ensembl transcript: ENST00000533348
  gene symbol: GSDMD
  hgvsc: ENST00000533348.1:c.450G>T
  hgvsp: ENST00000533348.1:c.450G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433958
  ensembl transcript: ENST00000533063
  gene symbol: GSDMD
  hgvsc: ENST00000533063.1:c.594G>T
  hgvsp: ENST00000533063.1:c.594G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000437065
  ensembl transcript: ENST00000533888
  gene symbol: GSDMD
  hgvsc: ENST00000533888.1:c.450G>T
  hgvsp: ENST00000533888.1:c.450G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000262580
  ensembl transcript: ENST00000262580
  gene symbol: GSDMD
  hgvsc: ENST00000262580.4:c.450G>T
  hgvsp: ENST00000262580.4:c.450G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000436684
  ensembl transcript: ENST00000534018
  gene symbol: GSDMD
  hgvsc: ENST00000534018.1:c.498G>T
  hgvsp: ENST00000534018.1:c.498G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104518
  ensembl protein: ENSP00000433209
  ensembl transcript: ENST00000526406
  gene symbol: GSDMD
  hgvsc: ENST00000526406.1:c.450G>T
  hgvsp: ENST00000526406.1:c.450G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000528475
  gene symbol: GSDMD
  hgvsc: ENST00000528475.1:n.603G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000531184
  gene symbol: GSDMD
  hgvsc: ENST00000531184.1:n.792G>T
  variant of: http://identifiers.org/hgnc/25697
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104518
  ensembl transcript: ENST00000526469
  gene symbol: GSDMD
  hgvsc: ENST00000526469.1:n.15G>T
  variant of: http://identifiers.org/hgnc/25697
canonical: true
consequence: synonymous
filter: PASS
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: 30
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7852
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 1.25e1
  variant carriers: 2
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: 35435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 2.25e1
  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: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu150Leu
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 255
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7320
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19086
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1403
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3800
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5326
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5760
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.560549313358302e-4
allele num: 6408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.38e-2

DP
type: SiteQuality
SIO_000300: 1.238355e6

VQSLOD
type: SiteQuality
SIO_000300: -1.603e0

QD
type: SiteQuality
SIO_000300: 1.221e1

GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 1590

GenotypeQuality
all individuals: 285
bin: 7.5e0
variant carriers: 265

GenotypeQuality
all individuals: 2137
bin: 7.25e1
variant carriers: 2136

GenotypeQuality
all individuals: 1393
bin: 2.75e1
variant carriers: 1377

GenotypeQuality
all individuals: 2423
bin: 8.25e1
variant carriers: 2423

GenotypeQuality
all individuals: 6839
bin: 9.75e1
variant carriers: 6839

GenotypeQuality
all individuals: 3131
bin: 7.75e1
variant carriers: 3130

GenotypeQuality
all individuals: 4606
bin: 6.75e1
variant carriers: 4604

GenotypeQuality
all individuals: 1067
bin: 8.75e1
variant carriers: 1067

GenotypeQuality
all individuals: 5495
bin: 6.25e1
variant carriers: 5461

GenotypeQuality
all individuals: 6496
bin: 5.25e1
variant carriers: 6496

GenotypeQuality
all individuals: 3036
bin: 4.25e1
variant carriers: 3034

African
type: Population
allele count: 7131
allele frequency: 8.160906385900664e-1
allele num: 8738
num of homozygotes: 2911

East Asian
type: Population
allele count: 7960
allele frequency: 1.0e0
allele num: 7960
num of homozygotes: 3980

European (Non-Finnish)
type: Population
allele count: 60524
allele frequency: 9.997357119259993e-1
allele num: 60540
num of homozygotes: 30254

Latino
type: Population
allele count: 10637
allele frequency: 9.935550158789463e-1
allele num: 10706
num of homozygotes: 5284

Other
type: Population
allele count: 815
allele frequency: 9.963325183374083e-1
allele num: 818
num of homozygotes: 406

European (Finnish)
type: Population
allele count: 5966
allele frequency: 1.0e0
allele num: 5966
num of homozygotes: 2983

South Asian
type: Population
allele count: 15928
allele frequency: 9.997489329651017e-1
allele num: 15932
num of homozygotes: 7962

MQ
type: SiteQuality
SIO_000300: 5.465e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: -1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.38e0

FS
type: SiteQuality
SIO_000300: 1.396e0

DP
type: SiteQuality
SIO_000300: 1.229129e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.792e-1

QD
type: SiteQuality
SIO_000300: 2.77e1

GenotypeQuality
all individuals: 829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21563
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1604
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17970
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.644675483525724e-5
allele num: 26162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10610
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

DP
type: SiteQuality
SIO_000300: 6.70122e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.061e1

FS
type: SiteQuality
SIO_000300: 1.381e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.213e0

MQRankSum
type: SiteQuality
SIO_000300: -1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.15e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.406e0

GenotypeQuality
all individuals: 26672
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3174
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

MQ
type: SiteQuality
SIO_000300: 5.301e1

FS
type: SiteQuality
SIO_000300: 2.377e0

DP
type: SiteQuality
SIO_000300: 5.66696e5

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.79e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.594e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 26672
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 12342
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 431
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 159
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 270
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 208
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 799
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19244
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.15059861373661e-4
allele num: 3174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1830
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 1.020199959192002e-3
allele num: 9802
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.301e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.79e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 2.377e0

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

MQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.594e1

DP
type: SiteQuality
SIO_000300: 5.66696e5

GenotypeQuality
all individuals: 3120
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 156
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3031
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 914
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30037
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.432498175626368e-4
allele num: 8222
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.45e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
type: SiteQuality
SIO_000300: -1.795e0

MQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.37e-2

DP
type: SiteQuality
SIO_000300: 3.67349e5

FS
type: SiteQuality
SIO_000300: 2.307e0

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30839
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 728
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3246
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.18962645729241e-4
allele num: 8406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1128
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.61374e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.254e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 3.442e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 225
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25771
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2525
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 99
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.595380223202699e-4
allele num: 7706
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.66109e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

QD
type: SiteQuality
SIO_000300: 3.099e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.690000000000001e-2

GenotypeQuality
all individuals: 2092
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3434
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 323
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.076923076923077e-3
allele num: 650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4200
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.649999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.5531e5

QD
type: SiteQuality
SIO_000300: 1.167e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQ
type: SiteQuality
SIO_000300: 5.395e1

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3600
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 235
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
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GenotypeQuality
all individuals: 1278
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7594
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.28488e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 5.604e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.35e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 8.73e0

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 133
bin: 2.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1611
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3622
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 287
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 749
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 213
bin: 9.75e1
variant carriers: 33

GenotypeQuality
all individuals: 82
bin: 8.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 5.113636363636364e-2
allele num: 176
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 7.926023778071334e-4
allele num: 7570
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 5.701754385964912e-2
allele num: 228
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.851851851851852e-3
allele num: 540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 8.32870627429206e-4
allele num: 3602
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.021e0

QD
type: SiteQuality
SIO_000300: 1.365e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.05e-1

DP
type: SiteQuality
SIO_000300: 2.07726e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.76e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 31

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 9

GenotypeQuality
all individuals: 211
bin: 2.75e1
variant carriers: 132

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 58

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 11

GenotypeQuality
all individuals: 127
bin: 7.25e1
variant carriers: 21

GenotypeQuality
all individuals: 71
bin: 9.25e1
variant carriers: 63

GenotypeQuality
all individuals: 198
bin: 1.75e1
variant carriers: 128

GenotypeQuality
all individuals: 126
bin: 7.75e1
variant carriers: 49

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 61

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 78

GenotypeQuality
all individuals: 2316
bin: 9.75e1
variant carriers: 2301

GenotypeQuality
all individuals: 79
bin: 8.25e1
variant carriers: 51

South Asian
type: Population
allele count: 1680
allele frequency: 2.214022140221402e-1
allele num: 7588
num of homozygotes: 201

European (Non-Finnish)
type: Population
allele count: 900
allele frequency: 2.465753424657534e-1
allele num: 3650
num of homozygotes: 109

European (Finnish)
type: Population
allele count: 5
allele frequency: 3.571428571428572e-1
allele num: 14
num of homozygotes: 1

Other
type: Population
allele count: 21
allele frequency: 1.567164179104478e-1
allele num: 134
num of homozygotes: 2

Latino
type: Population
allele count: 47
allele frequency: 2.526881720430108e-1
allele num: 186
num of homozygotes: 6

African
type: Population
allele count: 119
allele frequency: 2.125e-1
allele num: 560
num of homozygotes: 10

East Asian
type: Population
allele count: 19
allele frequency: 8.11965811965812e-2
allele num: 234
num of homozygotes: 1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.583e1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.57e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.39e-1

DP
type: SiteQuality
SIO_000300: 2.24306e5

GenotypeQuality
all individuals: 1265
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11846
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3586
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.318565400843882e-4
allele num: 7584
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.92195e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.31e-2

FS
type: SiteQuality
SIO_000300: 3.737e0

QD
type: SiteQuality
SIO_000300: 8.34e0

VQSLOD
type: SiteQuality
SIO_000300: -1.699e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.317e0

MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4154
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.317523056653491e-4
allele num: 7590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3576
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.290000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

FS
type: SiteQuality
SIO_000300: 6.153e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.038e-1

QD
type: SiteQuality
SIO_000300: 9.32e0

MQ
type: SiteQuality
SIO_000300: 5.672e1

DP
type: SiteQuality
SIO_000300: 1.90568e5

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 8.75e1
variant carriers: 1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7584
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 1.094890510948905e-2
allele num: 548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3584
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.914e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.222e0

VQSLOD
type: SiteQuality
SIO_000300: -1.04e0

FS
type: SiteQuality
SIO_000300: 7.581e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.610000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

DP
type: SiteQuality
SIO_000300: 1.80338e5

GenotypeQuality
all individuals: 16
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 494
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 194
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 152
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6745
bin: 7.5e0
variant carriers: 16

GenotypeQuality
all individuals: 731
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 238
bin: 9.75e1
variant carriers: 206

Latino
type: Population
allele count: 6
allele frequency: 3.448275862068965e-2
allele num: 174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 147
allele frequency: 4.076539101497504e-2
allele num: 3606
num of homozygotes: 3

Other
type: Population
allele count: 5
allele frequency: 3.90625e-2
allele num: 128
num of homozygotes: 0

South Asian
type: Population
allele count: 47
allele frequency: 6.213643574828133e-3
allele num: 7564
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.831501831501832e-2
allele num: 546
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.58e-2

DP
type: SiteQuality
SIO_000300: 1.75465e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.587e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 1.183e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.341e1

GenotypeQuality
all individuals: 44
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5358
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.639915522703273e-4
allele num: 7576
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.004e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.06e-1

DP
type: SiteQuality
SIO_000300: 1.6941e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.51e-2

GenotypeQuality
all individuals: 4900
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.317175974710221e-4
allele num: 7592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.51e-1

FS
type: SiteQuality
SIO_000300: 4.821e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.48e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.418e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.773e1

VQSLOD
type: SiteQuality
SIO_000300: -9.862e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

DP
type: SiteQuality
SIO_000300: 1.68407e5

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4298
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 42
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3646
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.316829075585989e-4
allele num: 7594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.498e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.29e-2

DP
type: SiteQuality
SIO_000300: 1.67781e5

MQRankSum
type: SiteQuality
SIO_000300: -3.506e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.391e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.113e0

FS
type: SiteQuality
SIO_000300: 5.17e0

QD
type: SiteQuality
SIO_000300: 5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.579e1

GenotypeQuality
all individuals: 4381
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 541
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 150
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4329
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.949447077409163e-4
allele num: 7596
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3640
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.753e0

QD
type: SiteQuality
SIO_000300: 9.02e0

MQ
type: SiteQuality
SIO_000300: 5.105e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.15e-2

DP
type: SiteQuality
SIO_000300: 1.67379e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.036e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.189e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.949447077409163e-4
allele num: 7596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.944e0

VQSLOD
type: SiteQuality
SIO_000300: -8.582e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.98e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.612e0

MQ
type: SiteQuality
SIO_000300: 5.193e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.13e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.950487226757967e-4
allele num: 7594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.85e-2

MQ
type: SiteQuality
SIO_000300: 5.273e1

FS
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.67412e5

QD
type: SiteQuality
SIO_000300: 1.426e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

VQSLOD
type: SiteQuality
SIO_000300: -1.758e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.388e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.71e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele count: 3
allele frequency: 3.948407475651487e-4
allele num: 7598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.179e0

QD
type: SiteQuality
SIO_000300: 1.408e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.84e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.019e0

FS
type: SiteQuality
SIO_000300: 6.117e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

DP
type: SiteQuality
SIO_000300: 1.67473e5

MQ
type: SiteQuality
SIO_000300: 5.233e1

GenotypeQuality
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bin: 1.25e1
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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GenotypeQuality
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GenotypeQuality
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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: 31
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GenotypeQuality
all individuals: 112
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.76056338028169e-3
allele num: 568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 1.69469e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.537e0

QD
type: SiteQuality
SIO_000300: 1.151e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: 5.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 4.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.768549280177187e-4
allele num: 3612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.88e-2

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.69452e5

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.243e0

VQSLOD
type: SiteQuality
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.768549280177187e-4
allele num: 3612
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

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

European (Non-Finnish)
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allele frequency: 2.793296089385475e-4
allele num: 3580
num of homozygotes: 0

East Asian
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VQSLOD
type: SiteQuality
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ClippingRankSum
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MQRankSum
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FS
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QD
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DP
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 3554
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African
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Latino
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South Asian
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VQSLOD
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QD
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FS
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MQ
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InbreedingCoeff
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DP
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GenotypeQuality
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bin: 3.75e1
variant carriers: 41

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 22
bin: 9.25e1
variant carriers: 21

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 36

GenotypeQuality
all individuals: 1936
bin: 9.75e1
variant carriers: 1929

African
type: Population
allele count: 118
allele frequency: 2.209737827715356e-1
allele num: 534
num of homozygotes: 10

European (Non-Finnish)
type: Population
allele count: 787
allele frequency: 2.70446735395189e-1
allele num: 2910
num of homozygotes: 96

Other
type: Population
allele count: 20
allele frequency: 2.040816326530612e-1
allele num: 98
num of homozygotes: 2

East Asian
type: Population
allele count: 15
allele frequency: 8.928571428571429e-2
allele num: 168
num of homozygotes: 1

South Asian
type: Population
allele count: 1584
allele frequency: 2.761506276150628e-1
allele num: 5736
num of homozygotes: 194

Latino
type: Population
allele count: 36
allele frequency: 2.278481012658228e-1
allele num: 158
num of homozygotes: 4

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.5e-1
allele num: 4
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

QD
type: SiteQuality
SIO_000300: 1.649e1

FS
type: SiteQuality
SIO_000300: 6.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.18e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

DP
type: SiteQuality
SIO_000300: 1.17538e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

GenotypeQuality
all individuals: 559
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2563
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.3801e4

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: -1.506e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.259e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

GenotypeQuality
all individuals: 490
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 261
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5451
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.507507507507507e-4
allele num: 1332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

FS
type: SiteQuality
SIO_000300: 9.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.588e0

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

DP
type: SiteQuality
SIO_000300: 6.2605e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.45e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.43e-2

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 354
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1070
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 7.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 94
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 988
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.341e0

FS
type: SiteQuality
SIO_000300: 4.95e0

DP
type: SiteQuality
SIO_000300: 5.1528e4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.249e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.820000000000001e-2

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 8.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 34
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.702e0

QD
type: SiteQuality
SIO_000300: 1.557e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.404e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.077e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.14e-2

DP
type: SiteQuality
SIO_000300: 4.9302e4

GenotypeQuality
all individuals: 9213
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 914
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.9435e4

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.409999999999999e-2

QD
type: SiteQuality
SIO_000300: 3.065e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.32e-1

GenotypeQuality
all individuals: 511
bin: 9.75e1
variant carriers: 509

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 24

GenotypeQuality
all individuals: 55
bin: 8.75e1
variant carriers: 55

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 49

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 59

GenotypeQuality
all individuals: 605
bin: 1.75e1
variant carriers: 588

GenotypeQuality
all individuals: 81
bin: 6.25e1
variant carriers: 46

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 27

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 83

GenotypeQuality
all individuals: 380
bin: 2.25e1
variant carriers: 313

GenotypeQuality
all individuals: 51
bin: 6.75e1
variant carriers: 41

GenotypeQuality
all individuals: 3580
bin: 7.5e0
variant carriers: 1097

GenotypeQuality
all individuals: 32
bin: 9.25e1
variant carriers: 32

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 106

Other
type: Population
allele count: 12
allele frequency: 6.0e-1
allele num: 20
num of homozygotes: 3

African
type: Population
allele count: 213
allele frequency: 5.489690721649485e-1
allele num: 388
num of homozygotes: 51

European (Non-Finnish)
type: Population
allele count: 584
allele frequency: 5.995893223819302e-1
allele num: 974
num of homozygotes: 169

Latino
type: Population
allele count: 52
allele frequency: 5.531914893617021e-1
allele num: 94
num of homozygotes: 12

European (Finnish)
type: Population
allele count: 6
allele frequency: 7.5e-1
allele num: 8
num of homozygotes: 2

South Asian
type: Population
allele count: 95
allele frequency: 6.597222222222222e-1
allele num: 144
num of homozygotes: 31

East Asian
type: Population
allele count: 81
allele frequency: 9.204545454545454e-1
allele num: 88
num of homozygotes: 38

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.881e1

QD
type: SiteQuality
SIO_000300: 2.506e1

FS
type: SiteQuality
SIO_000300: 5.26e-1

DP
type: SiteQuality
SIO_000300: 5.6488e4

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.641e-1

GenotypeQuality
all individuals: 46
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14305
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 25
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 150
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 2.73224043715847e-3
allele num: 366
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.114164904862579e-3
allele num: 946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.58e1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.81e-2

DP
type: SiteQuality
SIO_000300: 5.6943e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 105

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

GenotypeQuality
all individuals: 37
bin: 7.75e1
variant carriers: 37

GenotypeQuality
all individuals: 99
bin: 6.25e1
variant carriers: 99

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

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 20

GenotypeQuality
all individuals: 86
bin: 9.75e1
variant carriers: 86

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 107

GenotypeQuality
all individuals: 4410
bin: 7.5e0
variant carriers: 4371

GenotypeQuality
all individuals: 34
bin: 7.25e1
variant carriers: 34

GenotypeQuality
all individuals: 357
bin: 2.25e1
variant carriers: 357

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 45

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

GenotypeQuality
all individuals: 31
bin: 8.25e1
variant carriers: 31

European (Non-Finnish)
type: Population
allele count: 1070
allele frequency: 1.0e0
allele num: 1070
num of homozygotes: 535

Other
type: Population
allele count: 18
allele frequency: 1.0e0
allele num: 18
num of homozygotes: 9

East Asian
type: Population
allele count: 106
allele frequency: 1.0e0
allele num: 106
num of homozygotes: 53

South Asian
type: Population
allele count: 130
allele frequency: 1.0e0
allele num: 130
num of homozygotes: 65

European (Finnish)
type: Population
allele count: 6
allele frequency: 1.0e0
allele num: 6
num of homozygotes: 3

Latino
type: Population
allele count: 96
allele frequency: 1.0e0
allele num: 96
num of homozygotes: 48

African
type: Population
allele count: 372
allele frequency: 9.393939393939394e-1
allele num: 396
num of homozygotes: 174

FS
type: SiteQuality
SIO_000300: 1.118e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.365e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 3.381e1

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

DP
type: SiteQuality
SIO_000300: 6.8715e4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 658
bin: 2.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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MQ
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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Latino
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European (Finnish)
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Other
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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Other
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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South Asian
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East Asian
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European (Finnish)
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Other
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VQSLOD
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BaseQRankSum
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DP
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MQRankSum
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ReadPosRankSum
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FS
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QD
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InbreedingCoeff
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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South Asian
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Latino
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African
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European (Finnish)
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East Asian
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQRankSum
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QD
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DP
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeQuality
all individuals: 12370
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 94
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36714
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 339
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.51e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.601e0

QD
type: SiteQuality
SIO_000300: 6.59e0

DP
type: SiteQuality
SIO_000300: 2.15578e5

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16133
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33292
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 470
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1408
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 9.345794392523365e-4
allele num: 2140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.229e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

DP
type: SiteQuality
SIO_000300: 2.51906e5

FS
type: SiteQuality
SIO_000300: 2.078e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-1

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2680
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1629
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 409
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16699
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.044989775051125e-3
allele num: 978
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2234
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.46e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.731e0

DP
type: SiteQuality
SIO_000300: 2.58566e5

QD
type: SiteQuality
SIO_000300: 1.221e1

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22010
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28929
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1958
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.690036900369004e-4
allele num: 2710
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

DP
type: SiteQuality
SIO_000300: 2.93166e5

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.79e-1

QD
type: SiteQuality
SIO_000300: 1.448e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.63e-2

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2212
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22378
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2832
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.49e-2

DP
type: SiteQuality
SIO_000300: 2.97594e5

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.267e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

QD
type: SiteQuality
SIO_000300: 1.787e1

GenotypeQuality
all individuals: 596
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2323
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25334
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3416
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 5.861664712778429e-4
allele num: 1706
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 930
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

DP
type: SiteQuality
SIO_000300: 3.22787e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.88e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.066000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

GenotypeQuality
all individuals: 265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2484
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1200
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.286e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.733e0

VQSLOD
type: SiteQuality
SIO_000300: -4.084e0

DP
type: SiteQuality
SIO_000300: 3.33551e5

QD
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

GenotypeQuality
all individuals: 1179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23220
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3870
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.427184466019417e-3
allele num: 412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1076
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.43235e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.46e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

QD
type: SiteQuality
SIO_000300: 5.39e0

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

GenotypeQuality
all individuals: 1519
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28365
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.27e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.139e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.09e0

DP
type: SiteQuality
SIO_000300: 3.53844e5

GenotypeQuality
all individuals: 18868
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.009646302250804e-4
allele num: 4976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.85134e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.75e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.54e-1

QD
type: SiteQuality
SIO_000300: 1.302e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.547987616099071e-3
allele num: 646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.48e-2

DP
type: SiteQuality
SIO_000300: 3.95525e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

QD
type: SiteQuality
SIO_000300: 9.09e0

MQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

GenotypeQuality
all individuals: 33917
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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: 1

GenotypeQuality
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GenotypeQuality
all individuals: 47
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5902
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3298
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.033e1

FS
type: SiteQuality
SIO_000300: 3.136e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.1e-3

DP
type: SiteQuality
SIO_000300: 4.12645e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.17e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 467
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 182
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GenotypeQuality
all individuals: 69
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1014
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 2.094240837696335e-3
allele num: 1910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.277791975466394e-4
allele num: 7826
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

FS
type: SiteQuality
SIO_000300: 1.985e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

QD
type: SiteQuality
SIO_000300: 1.085e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 4.58665e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 301
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1946
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4724
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.487666034155598e-4
allele num: 1054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.728e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

DP
type: SiteQuality
SIO_000300: 4.66871e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.395e0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: -1.568e0

QD
type: SiteQuality
SIO_000300: 9.33e0

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1088
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.74595e5

VQSLOD
type: SiteQuality
SIO_000300: -1.529e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.08e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

QD
type: SiteQuality
SIO_000300: 7.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

FS
type: SiteQuality
SIO_000300: 9.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.33590282644242e-4
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1108
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2046
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.08e-2

FS
type: SiteQuality
SIO_000300: 9.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.529e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.74595e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1486
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.949852507374631e-4
allele num: 6780
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.07e-2

QD
type: SiteQuality
SIO_000300: 1.067e1

DP
type: SiteQuality
SIO_000300: 5.28522e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2192
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.6249593760156e-4
allele num: 12308
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -5.076000000000001e-1

InbreedingCoeff
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ClippingRankSum
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MQ
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QD
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DP
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -1.092e0

MQRankSum
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SIO_000300: 8.169999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.124e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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DP
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FS
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MQ
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VQSLOD
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SIO_000300: -1.746e0

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

European (Non-Finnish)
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allele frequency: 1.166180758017493e-3
allele num: 13720
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South Asian
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allele frequency: 0.0e0
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Latino
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East Asian
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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DP
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MQ
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 14390
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.81e-2

VQSLOD
type: SiteQuality
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MQRankSum
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ClippingRankSum
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DP
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QD
type: SiteQuality
SIO_000300: 1.363e1

BaseQRankSum
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SIO_000300: -1.589e0

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 3.289473684210526e-3
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Latino
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 7.29e-1

ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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MQ
type: SiteQuality
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FS
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DP
type: SiteQuality
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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European (Finnish)
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South Asian
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Other
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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FS
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QD
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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