7-87810795-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810795
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810795
    reference: chr 7
allele count: 2
allele frequency: 1.762611485176437e-5
allele num: 113468
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.394-25A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2283-7A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.483-25A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2310-25A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2409-25A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2409-25A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2301-25A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2301-25A>G
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9463
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5148
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3622
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 3.75e1
  variant carriers: 0
hgvs: c.2283-7A>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

7-87810800-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810800
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810800
    reference: chr 7
allele count: 1
allele frequency: 8.691722003963425e-6
allele num: 115052
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.394-20A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2301-20A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2283-2A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2409-20A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2301-20A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.483-20A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2409-20A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2310-20A>G
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2283-2A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-87810802-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810802
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810802
    reference: chr 7
allele count: 3
allele frequency: 2.595200609007076e-5
allele num: 115598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.483-18C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2310-18C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.394-18C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2301-18C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2283C>G
  hgvsp: ENSP00000315900.7:p.Asn761Lys
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2409-18C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2301-18C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2409-18C>G
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10132
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1841
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2574
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn761Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

7-87810810-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810810
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810809
    reference: chr 7
allele count: 1
allele frequency: 8.490838385382172e-6
allele num: 117774
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2409-9delC
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.394-9delC
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2301-9delC
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.483-9delC
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2292delC
  hgvsp: ENSP00000315900.7:p.Phe764LeufsTer62
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2409-9delC
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2310-9delC
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2301-9delC
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38930
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1542
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe764LeufsTer62
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: TC
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

7-87810820-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810820
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810820
    reference: chr 7
allele count: 1
allele frequency: 8.36470096194061e-6
allele num: 119550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2310G>A
  hgvsp: ENST00000398203.3:c.2310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.483G>A
  hgvsp: ENST00000426930.1:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2409G>A
  hgvsp: ENST00000398201.4:c.2409G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2301G>A
  hgvsp: ENST00000398204.4:c.2301G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2301G>A
  hgvsp: ENST00000398209.3:c.2301G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.394G>A
  hgvsp: ENST00000413139.1:c.394G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2409G>A
  hgvsp: ENST00000265727.7:c.2409G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2301G>A
  hgvsp: ENST00000315984.7:c.2301G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5464
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: c.2409G>A
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-87810827-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810827
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810827
    reference: chr 7
allele count: 1
allele frequency: 8.332777814812346e-6
allele num: 120008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2317G>T
  hgvsp: ENSP00000381261.3:p.Gly773Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2308G>T
  hgvsp: ENSP00000381262.4:p.Gly770Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2308G>T
  hgvsp: ENSP00000381267.3:p.Gly770Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.490G>T
  hgvsp: ENSP00000396233.1:p.Gly164Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.401G>T
  hgvsp: ENSP00000412085.1:p.Gly135Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2416G>T
  hgvsp: ENSP00000381260.4:p.Gly806Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2308G>T
  hgvsp: ENSP00000315900.7:p.Gly770Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2416G>T
  hgvsp: ENSP00000265727.7:p.Gly806Trp
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43215
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5149
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly806Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

7-87810871-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810871
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810871
    reference: chr 7
allele count: 2
allele frequency: 1.661046791688122e-5
allele num: 120406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2460T>C
  hgvsp: ENST00000398201.4:c.2460T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2361T>C
  hgvsp: ENST00000398203.3:c.2361T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2352T>C
  hgvsp: ENST00000398209.3:c.2352T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2352T>C
  hgvsp: ENST00000398204.4:c.2352T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.445T>C
  hgvsp: ENST00000413139.1:c.445T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.534T>C
  hgvsp: ENST00000426930.1:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2352T>C
  hgvsp: ENST00000315984.7:c.2352T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2460T>C
  hgvsp: ENST00000265727.7:c.2460T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43437
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
hgvs: p.His820His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

7-87810881-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810881
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810881
    reference: chr 7
allele count: 3
allele frequency: 2.493433957245919e-5
allele num: 120316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.544A>T
  hgvsp: ENSP00000396233.1:p.Ile182Phe
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2470A>T
  hgvsp: ENSP00000381260.4:p.Ile824Phe
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2371A>T
  hgvsp: ENSP00000381261.3:p.Ile791Phe
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2362A>T
  hgvsp: ENSP00000381262.4:p.Ile788Phe
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.455A>T
  hgvsp: ENSP00000412085.1:p.Ile153Phe
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2362A>T
  hgvsp: ENSP00000315900.7:p.Ile788Phe
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2362A>T
  hgvsp: ENSP00000381267.3:p.Ile788Phe
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2470A>T
  hgvsp: ENSP00000265727.7:p.Ile824Phe
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile824Phe
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

7-87810882-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810882
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810882
    reference: chr 7
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2372T>G
  hgvsp: ENSP00000381261.3:p.Ile791Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2363T>G
  hgvsp: ENSP00000381262.4:p.Ile788Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2471T>G
  hgvsp: ENSP00000265727.7:p.Ile824Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.545T>G
  hgvsp: ENSP00000396233.1:p.Ile182Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2363T>G
  hgvsp: ENSP00000381267.3:p.Ile788Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2471T>G
  hgvsp: ENSP00000381260.4:p.Ile824Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.456T>G
  hgvsp: ENSP00000412085.1:p.Ile153Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2363T>G
  hgvsp: ENSP00000315900.7:p.Ile788Ser
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile824Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

7-87810898-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810898
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810898
    reference: chr 7
allele count: 1
allele frequency: 8.331666999933347e-6
allele num: 120024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2379A>T
  hgvsp: ENST00000398209.3:c.2379A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2379A>T
  hgvsp: ENST00000315984.7:c.2379A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.472A>T
  hgvsp: ENST00000413139.1:c.472A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.561A>T
  hgvsp: ENST00000426930.1:c.561A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2487A>T
  hgvsp: ENST00000398201.4:c.2487A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2379A>T
  hgvsp: ENST00000398204.4:c.2379A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2487A>T
  hgvsp: ENST00000265727.7:c.2487A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381261
  ensembl transcript: ENST00000398203
  gene symbol: ADAM22
  hgvsc: ENST00000398203.3:c.2388A>T
  hgvsp: ENST00000398203.3:c.2388A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg829Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

7-87810954-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810954
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810954
    reference: chr 7
allele count: 1
allele frequency: 8.489685032685287e-6
allele num: 117790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.494+34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.583+34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2509+34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2401+34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2509+34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2401+34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2401+34A>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5930
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10332
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3598
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1850
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

7-87810955-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810955
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810955
    reference: chr 7
allele count: 20812
allele frequency: 1.77437506394298e-1
allele num: 117292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2509+35T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2401+35T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2509+35T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2401+35T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2401+35T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.583+35T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.494+35T>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.5e0
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 21011
  bin: 2.25e1
  variant carriers: 2734
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 1.25e1
  variant carriers: 740
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 1.75e1
  variant carriers: 1813
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 1555
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 3.25e1
  variant carriers: 2949
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 9.75e1
  variant carriers: 533
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 174
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.75e1
  variant carriers: 875
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 3.75e1
  variant carriers: 2282
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 2.75e1
  variant carriers: 3204
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.75e1
  variant carriers: 213
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 440
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.25e1
  variant carriers: 108
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 5.75e1
  variant carriers: 129
genotype quality: GenotypeQuality
  all individuals: 3236
  bin: 6.75e1
  variant carriers: 232
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 8.75e1
  variant carriers: 139
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 3.75e1
  variant carriers: 75
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 8.25e1
  variant carriers: 238
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.5e0
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 2476
  bin: 3.25e1
  variant carriers: 61
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 4.25e1
  variant carriers: 63
num of homozygotes: 2859
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ

7-87810957-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87810957
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87810957
    reference: chr 7
allele count: 2
allele frequency: 1.711127461884636e-5
allele num: 116882
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.583+37A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2401+37A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.494+37A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2401+37A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2509+37A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2509+37A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2401+37A>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19504
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9078
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2059
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1646
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5527
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4816
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4524
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3820
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

7-87811223-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811223
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811223
    reference: chr 7
allele count: 1
allele frequency: 8.462814393554721e-6
allele num: 118164
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-50G>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-50G>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-50G>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-50G>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-50G>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-50G>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-50G>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6567
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4579
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/7-87811226-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811226
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811226
    reference: chr 7
allele count: 1
allele frequency: 8.466110161025414e-6
allele num: 118118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-47C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-47C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-47C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-47C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-47C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-47C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-47C>A
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7339
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16453
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6636
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1207
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-87811231-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811231
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811231
    reference: chr 7
allele count: 130
allele frequency: 1.098121367752399e-3
allele num: 118384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-42A>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10956
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7458
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11988
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 5.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 3726
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6744
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

7-87811240-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811240
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811240
    reference: chr 7
allele count: 1
allele frequency: 8.43340979624882e-6
allele num: 118576
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-33C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-33C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-33C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-33C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-33C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-33C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-33C>T
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2968
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3736
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1903
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-87811241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811241
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811241
    reference: chr 7
allele count: 1
allele frequency: 8.425735566714975e-6
allele num: 118684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-32A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-32A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-32A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-32A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-32A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-32A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-32A>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

7-87811242-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811242
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811242
    reference: chr 7
allele count: 1
allele frequency: 8.425735566714975e-6
allele num: 118684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-31T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-31T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-31T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-31T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-31T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-31T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-31T>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6845
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16436
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4544
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3021
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2969
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-87811256-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811256
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811256
    reference: chr 7
allele count: 1
allele frequency: 8.389261744966442e-6
allele num: 119200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-17T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-17T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-17T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-17T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-17T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-17T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-17T>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2970
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4550
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

7-87811257-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811257
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811257
    reference: chr 7
allele count: 1
allele frequency: 8.384619254439656e-6
allele num: 119266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-16A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-16A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-16A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-16A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-16A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-16A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-16A>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16436
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2970
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

7-87811261-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811261
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811261
    reference: chr 7
allele count: 3
allele frequency: 2.51302585065925e-5
allele num: 119378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-12C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-12C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-12C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-12C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-12C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-12C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-12C>T
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12954
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4548
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19118
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1906
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

7-87811262-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811262
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811262
    reference: chr 7
allele count: 9
allele frequency: 7.53465943339361e-5
allele num: 119448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.584-11G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2510-11G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2510-11G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2402-11G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.495-11G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2402-11G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2402-11G>A
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2968
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16440
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6989
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-87811302-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811302
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811302
    reference: chr 7
allele count: 1
allele frequency: 8.344041519950603e-6
allele num: 119846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2431A>G
  hgvsp: ENSP00000381262.4:p.Arg811Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.524A>G
  hgvsp: ENSP00000412085.1:p.Arg176Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2539A>G
  hgvsp: ENSP00000265727.7:p.Arg847Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2539A>G
  hgvsp: ENSP00000381260.4:p.Arg847Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.613A>G
  hgvsp: ENSP00000396233.1:p.Arg205Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2431A>G
  hgvsp: ENSP00000315900.7:p.Arg811Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2431A>G
  hgvsp: ENSP00000381267.3:p.Arg811Gly
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13328
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16436
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7037
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19750
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3737
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg847Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/7-87811308-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811308
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811308
    reference: chr 7
allele count: 1
allele frequency: 8.347942232239753e-6
allele num: 119790
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.619A>C
  hgvsp: ENSP00000396233.1:p.Lys207Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2545A>C
  hgvsp: ENSP00000265727.7:p.Lys849Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2437A>C
  hgvsp: ENSP00000381267.3:p.Lys813Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.530A>C
  hgvsp: ENSP00000412085.1:p.Lys178Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2437A>C
  hgvsp: ENSP00000381262.4:p.Lys813Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2437A>C
  hgvsp: ENSP00000315900.7:p.Lys813Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2545A>C
  hgvsp: ENSP00000381260.4:p.Lys849Gln
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7332
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3735
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19754
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys849Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

7-87811323-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811323
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811323
    reference: chr 7
allele count: 2
allele frequency: 1.672716324038606e-5
allele num: 119566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.634C>T
  hgvsp: ENSP00000396233.1:p.Arg212Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2560C>T
  hgvsp: ENSP00000381260.4:p.Arg854Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2452C>T
  hgvsp: ENSP00000315900.7:p.Arg818Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2452C>T
  hgvsp: ENSP00000381262.4:p.Arg818Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.545C>T
  hgvsp: ENSP00000412085.1:p.Arg183Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.4C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2560C>T
  hgvsp: ENSP00000265727.7:p.Arg854Trp
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2452C>T
  hgvsp: ENSP00000381267.3:p.Arg818Trp
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2965
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4530
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19430
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg854Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ

7-87811324-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811324
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811324
    reference: chr 7
allele count: 4
allele frequency: 3.345824411134904e-5
allele num: 119552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2453G>A
  hgvsp: ENSP00000315900.7:p.Arg818Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2453G>A
  hgvsp: ENSP00000381262.4:p.Arg818Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.546G>A
  hgvsp: ENSP00000412085.1:p.Arg183Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2453G>A
  hgvsp: ENSP00000381267.3:p.Arg818Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.5G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2561G>A
  hgvsp: ENSP00000265727.7:p.Arg854Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.2561G>A
  hgvsp: ENSP00000381260.4:p.Arg854Gln
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.635G>A
  hgvsp: ENSP00000396233.1:p.Arg212Gln
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10488
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19462
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3730
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg854Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

7-87811345-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811345
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811345
    reference: chr 7
allele count: 1
allele frequency: 8.38940250675347e-6
allele num: 119198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.*2T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+6T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+6T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+6T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+6T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.650+6T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+6T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.20+6T>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18517
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6918
  bin: 6.75e1
  variant carriers: 0
hgvs: c.2576+6T>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

7-87811357-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811357
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811357
    reference: chr 7
allele count: 309
allele frequency: 2.598691403293358e-3
allele num: 118906
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+18A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+18A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+18A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+18A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+18A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.20+18A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.650+18A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.*14A>G
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7306
  bin: 3.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 8755
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12907
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 5.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 4.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 4.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 11095
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4478
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

7-87811367-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811367
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811367
    reference: chr 7
allele count: 1
allele frequency: 8.432840855427377e-6
allele num: 118584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+28G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+28G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.*24G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+28G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.650+28G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.20+28G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+28G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+28G>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15905
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

7-87811376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811376
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811376
    reference: chr 7
allele count: 1
allele frequency: 8.449656943928076e-6
allele num: 118348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+37G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.*33G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+37G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.20+37G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+37G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+37G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.650+37G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+37G>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7279
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3649
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2146
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

7-87811377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811377
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811377
    reference: chr 7
allele count: 1
allele frequency: 8.451085119329322e-6
allele num: 118328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+38G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.20+38G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.650+38G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+38G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+38G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+38G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.*34G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+38G>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13852
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2871
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3648
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1605
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

7-87811383-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811383
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811383
    reference: chr 7
allele count: 5
allele frequency: 4.235636955085306e-5
allele num: 118046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+44T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+44T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.*40T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.650+44T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.20+44T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+44T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+44T>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+44T>G
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11322
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5985
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4315
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

7-87811393-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87811393
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87811393
    reference: chr 7
allele count: 1
allele frequency: 8.518758305789349e-6
allele num: 117388
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+54G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+54G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.650+54G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+54G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+54G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+54G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381260
  ensembl transcript: ENST00000398201
  gene symbol: ADAM22
  hgvsc: ENST00000398201.4:c.*50G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.20+54G>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2607
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4196
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/7-87813573-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87813573
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87813573
    reference: chr 7
allele count: 3
allele frequency: 3.913383772501957e-4
allele num: 7666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+2234C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+2234C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+2234C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.21-1572C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+2234C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.651-34C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+2234C>A
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2358
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

7-87813616-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87813616
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87813616
    reference: chr 7
allele count: 1
allele frequency: 8.440243079000676e-5
allele num: 11848
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.660C>G
  hgvsp: ENST00000426930.1:c.660C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+2277C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+2277C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.21-1529C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+2277C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+2277C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+2277C>G
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro220Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

7-87813619-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87813619
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87813619
    reference: chr 7
allele count: 1
allele frequency: 8.225037012666557e-5
allele num: 12158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.21-1526A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+2280A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.663A>G
  hgvsp: ENST00000426930.1:c.663A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+2280A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+2280A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+2280A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+2280A>G
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln221Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

7-87813620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87813620
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87813620
    reference: chr 7
allele count: 1
allele frequency: 8.173941474579042e-5
allele num: 12234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.561+2281G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.664G>A
  hgvsp: ENSP00000396233.1:p.Ala222Thr
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2468+2281G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.21-1525G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2468+2281G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+2281G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+2281G>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4200
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala222Thr
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

7-87813635-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87813635
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87813635
    reference: chr 7
allele count: 2832
allele frequency: 2.081128747795414e-1
allele num: 13608
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2469-2295C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2469-2295C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.679C>T
  hgvsp: ENSP00000396233.1:p.His227Tyr
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.21-1510C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+2296C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+2296C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.562-2295C>T
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 2.25e1
  variant carriers: 379
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 2.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.75e1
  variant carriers: 391
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 3.25e1
  variant carriers: 473
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 234
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.75e1
  variant carriers: 479
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 2.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1316
  bin: 7.5e0
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 9.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 15
hgvs: p.His227Tyr
num of homozygotes: 356
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

7-87813644-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87813644
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87813644
    reference: chr 7
allele count: 2
allele frequency: 1.466490687784132e-4
allele num: 13638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2469-2286G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2469-2286G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.21-1501G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.688G>A
  hgvsp: ENSP00000396233.1:p.Ala230Thr
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.562-2286G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+2305G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+2305G>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala230Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

7-87813649-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87813649
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87813649
    reference: chr 7
allele count: 1
allele frequency: 7.307804735457468e-5
allele num: 13684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.693G>A
  hgvsp: ENST00000426930.1:c.693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+2310G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2469-2281G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2469-2281G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.562-2281G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.21-1496G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+2310G>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln231Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-87813728-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87813728
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87813728
    reference: chr 7
allele count: 1
allele frequency: 9.790483649892304e-5
allele num: 10214
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+2389A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.562-2202A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+2389A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2469-2202A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.761+11A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.21-1417A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2469-2202A>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  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: 2710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2087
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3003
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/7-87813766-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87813766
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87813766
    reference: chr 7
allele count: 1395
allele frequency: 1.850623507561688e-1
allele num: 7538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.562-2164A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl transcript: ENST00000476330
  gene symbol: ADAM22
  hgvsc: ENST00000476330.1:n.21-1379A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2469-2164A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+2427A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.761+49A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2469-2164A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+2427A>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 3.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 2.5e0
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 3.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 1.25e1
  variant carriers: 811
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 7.5e0
  variant carriers: 901
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.75e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 1207
  bin: 9.75e1
  variant carriers: 1119
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 1.75e1
  variant carriers: 110
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.75e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 3.25e1
  variant carriers: 77
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 6.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.25e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 7.5e0
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 2.75e1
  variant carriers: 54
num of homozygotes: 163
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-87815883-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815883
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815883
    reference: chr 7
allele count: 4
allele frequency: 3.314331167970303e-5
allele num: 120688
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2469-47T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.762-47T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4544T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.562-47T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4544T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2469-47T>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2510
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4114
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2703
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD

7-87815887-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815887
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815887
    reference: chr 7
allele count: 1
allele frequency: 8.285278716776033e-6
allele num: 120696
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4548T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2469-43T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2469-43T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.762-43T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4548T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.562-43T>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37508
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

7-87815888-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815888
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815888
    reference: chr 7
allele count: 1
allele frequency: 8.286789200656313e-6
allele num: 120674
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.562-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4549A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2469-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.762-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2469-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4549A>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10449
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

7-87815889-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815889
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815889
    reference: chr 7
allele count: 1
allele frequency: 8.2847295864263e-6
allele num: 120704
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.762-41T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2469-41T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2469-41T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4550T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4550T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.562-41T>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17866
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10452
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2512
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1483
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

7-87815933-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815933
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815933
    reference: chr 7
allele count: 6
allele frequency: 4.969520275642725e-5
allele num: 120736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4594T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.565T>C
  hgvsp: ENST00000413139.1:c.565T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2472T>C
  hgvsp: ENST00000398209.3:c.2472T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.765T>C
  hgvsp: ENST00000426930.1:c.765T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4594T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2472T>C
  hgvsp: ENST00000315984.7:c.2472T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2509
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10454
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr824Tyr
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-87815940-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815940
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815940
    reference: chr 7
allele count: 2
allele frequency: 1.656506758547575e-5
allele num: 120736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2479C>A
  hgvsp: ENSP00000381267.3:p.Pro827Thr
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4601C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.772C>A
  hgvsp: ENSP00000396233.1:p.Pro258Thr
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.572C>A
  hgvsp: ENSP00000412085.1:p.Pro192Thr
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2479C>A
  hgvsp: ENSP00000315900.7:p.Pro827Thr
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4601C>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10454
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro827Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

7-87815940-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815940
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815940
    reference: chr 7
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4601C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2479C>T
  hgvsp: ENSP00000381267.3:p.Pro827Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.772C>T
  hgvsp: ENSP00000396233.1:p.Pro258Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.572C>T
  hgvsp: ENSP00000412085.1:p.Pro192Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2479C>T
  hgvsp: ENSP00000315900.7:p.Pro827Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4601C>T
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro827Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

7-87815942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815942
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815942
    reference: chr 7
allele count: 8
allele frequency: 6.626027034190299e-5
allele num: 120736
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.574A>G
  hgvsp: ENST00000413139.1:c.574A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4603A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2481A>G
  hgvsp: ENST00000315984.7:c.2481A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2481A>G
  hgvsp: ENST00000398209.3:c.2481A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.774A>G
  hgvsp: ENST00000426930.1:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4603A>G
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4097
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro827Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

7-87815945-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815945
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815945
    reference: chr 7
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2484G>A
  hgvsp: ENSP00000381267.3:p.Trp828Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.577G>A
  hgvsp: ENSP00000412085.1:p.Trp193Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4606G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4606G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2484G>A
  hgvsp: ENSP00000315900.7:p.Trp828Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.777G>A
  hgvsp: ENSP00000396233.1:p.Trp259Ter
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37678
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Trp828Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

7-87815946-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815946
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815946
    reference: chr 7
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.778T>C
  hgvsp: ENSP00000396233.1:p.Phe260Leu
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2485T>C
  hgvsp: ENSP00000381267.3:p.Phe829Leu
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4607T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2485T>C
  hgvsp: ENSP00000315900.7:p.Phe829Leu
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.578T>C
  hgvsp: ENSP00000412085.1:p.Phe194Leu
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4607T>C
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Phe829Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

7-87815949-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815949
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815949
    reference: chr 7
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.781A>T
  hgvsp: ENSP00000396233.1:p.Lys261Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.581A>T
  hgvsp: ENSP00000412085.1:p.Lys195Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2488A>T
  hgvsp: ENSP00000381267.3:p.Lys830Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2488A>T
  hgvsp: ENSP00000315900.7:p.Lys830Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4610A>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4610A>T
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2510
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys830Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

7-87815952-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815952
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815952
    reference: chr 7
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.784A>G
  hgvsp: ENSP00000396233.1:p.Arg262Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2491A>G
  hgvsp: ENSP00000381267.3:p.Arg831Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4613A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2491A>G
  hgvsp: ENSP00000315900.7:p.Arg831Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.584A>G
  hgvsp: ENSP00000412085.1:p.Arg196Gly
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4613A>G
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4086
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2510
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg831Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

7-87815957-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815957
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815957
    reference: chr 7
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2496C>T
  hgvsp: ENST00000315984.7:c.2496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.589C>T
  hgvsp: ENST00000413139.1:c.589C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4618C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4618C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.789C>T
  hgvsp: ENST00000426930.1:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2496C>T
  hgvsp: ENST00000398209.3:c.2496C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4085
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10459
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2510
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp832Asp
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

7-87815963-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815963
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815963
    reference: chr 7
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.795T>C
  hgvsp: ENST00000426930.1:c.795T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2502T>C
  hgvsp: ENST00000315984.7:c.2502T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.595T>C
  hgvsp: ENST00000413139.1:c.595T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4624T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4624T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2502T>C
  hgvsp: ENST00000398209.3:c.2502T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37684
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2510
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn834Asn
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

7-87815974-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815974
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815974
    reference: chr 7
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4635G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2513G>A
  hgvsp: ENSP00000315900.7:p.Trp838Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.606G>A
  hgvsp: ENSP00000412085.1:p.Trp203Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.806G>A
  hgvsp: ENSP00000396233.1:p.Trp269Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2513G>A
  hgvsp: ENSP00000381267.3:p.Trp838Ter
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4635G>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37680
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10456
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Trp838Ter
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

7-87815975-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815975
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815975
    reference: chr 7
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2514G>C
  hgvsp: ENSP00000315900.7:p.Trp838Cys
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4636G>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.807G>C
  hgvsp: ENSP00000396233.1:p.Trp269Cys
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4636G>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2514G>C
  hgvsp: ENSP00000381267.3:p.Trp838Cys
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.607G>C
  hgvsp: ENSP00000412085.1:p.Trp203Cys
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4083
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10456
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Trp838Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

7-87815995-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87815995
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87815995
    reference: chr 7
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4656A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.627A>G
  hgvsp: ENSP00000412085.1:p.Asn210Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.827A>G
  hgvsp: ENSP00000396233.1:p.Asn276Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4656A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2534A>G
  hgvsp: ENSP00000381267.3:p.Asn845Ser
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2534A>G
  hgvsp: ENSP00000315900.7:p.Asn845Ser
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2506
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn845Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum

7-87816000-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87816000
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87816000
    reference: chr 7
allele count: 1
allele frequency: 8.288987251537607e-6
allele num: 120642
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4661G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2539G>A
  hgvsp: ENSP00000315900.7:p.Glu847Lys
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2539G>A
  hgvsp: ENSP00000381267.3:p.Glu847Lys
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.832G>A
  hgvsp: ENSP00000396233.1:p.Glu278Lys
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4661G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.632G>A
  hgvsp: ENSP00000412085.1:p.Glu212Lys
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37576
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2503
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu847Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

7-87816004-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87816004
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87816004
    reference: chr 7
allele count: 28
allele frequency: 2.322726216942629e-4
allele num: 120548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.836G>A
  hgvsp: ENSP00000396233.1:p.Gly279Glu
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2543G>A
  hgvsp: ENSP00000381267.3:p.Gly848Glu
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4665G>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2543G>A
  hgvsp: ENSP00000315900.7:p.Gly848Glu
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.636G>A
  hgvsp: ENSP00000412085.1:p.Gly213Glu
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4665G>A
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 22860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 37503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly848Glu
num of homozygotes: 1
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

7-87816023-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87816023
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87816023
    reference: chr 7
allele count: 1
allele frequency: 8.383775717232013e-6
allele num: 119278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2555+7T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4684T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.848+7T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.648+7T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2555+7T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4684T>C
  variant of: http://identifiers.org/hgnc/201
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36231
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9990
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 9.25e1
  variant carriers: 0
hgvs: c.2555+7T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

7-87816025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87816025
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87816025
    reference: chr 7
allele count: 1
allele frequency: 8.411985396793351e-6
allele num: 118878
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2555+9T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4686T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2555+9T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.648+9T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4686T>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.848+9T>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2572
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9804
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

7-87816030-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87816030
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87816030
    reference: chr 7
allele count: 1
allele frequency: 8.503256747334228e-6
allele num: 117602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2555+14T>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.848+14T>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4691T>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.648+14T>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2555+14T>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4691T>A
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8934
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3512
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33673
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/7-87816032-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87816032
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87816032
    reference: chr 7
allele count: 2
allele frequency: 1.703954879274797e-5
allele num: 117374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.648+16A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.848+16A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2555+16A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4693A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4693A>C
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2555+16A>C
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

7-87816052-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87816052
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87816052
    reference: chr 7
allele count: 1
allele frequency: 8.797705558390373e-6
allele num: 113666
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2555+36C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2555+36C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4713C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.848+36C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4713C>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.648+36C>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
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genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
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genotype depth: GenotypeDepth
  all individuals: 2059
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genotype depth: GenotypeDepth
  all individuals: 133
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genotype depth: GenotypeDepth
  all individuals: 99
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genotype depth: GenotypeDepth
  all individuals: 96
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genotype quality: GenotypeQuality
  all individuals: 325
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 580
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genotype quality: GenotypeQuality
  all individuals: 94
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genotype quality: GenotypeQuality
  all individuals: 6514
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 4552
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genotype quality: GenotypeQuality
  all individuals: 4031
  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1027
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5616
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

7-87816061-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87816061
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87816061
    reference: chr 7
allele count: 2
allele frequency: 1.788524824724567e-5
allele num: 111824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.648+45C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2555+45C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2555+45C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.848+45C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2468+4722C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2576+4722C>T
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 10468
  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 14904
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4413
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 9783
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genotype depth: GenotypeDepth
  all individuals: 96
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 365
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genotype quality: GenotypeQuality
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

7-87822389-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87822389
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87822389
    reference: chr 7
allele count: 2
allele frequency: 1.659475605708596e-5
allele num: 120520
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2577-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2469-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.849-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2556-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.649-42A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2556-42A>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2750
  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-87822392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87822392
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87822392
    reference: chr 7
allele count: 1
allele frequency: 8.298479718515568e-6
allele num: 120504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.649-39C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2469-39C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2556-39C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.849-39C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2556-39C>T
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2577-39C>T
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30359
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2566
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39185
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

7-87822397-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87822397
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87822397
    reference: chr 7
allele count: 1
allele frequency: 8.292148993333113e-6
allele num: 120596
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2469-34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2556-34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2577-34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.849-34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2556-34A>G
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.649-34A>G
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1399
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9674
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2604
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2566
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-87822405-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 87822405
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 87822405
    reference: chr 7
allele count: 30
allele frequency: 2.487232207998939e-4
allele num: 120616
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000315900
  ensembl transcript: ENST00000315984
  gene symbol: ADAM22
  hgvsc: ENST00000315984.7:c.2556-26C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000396233
  ensembl transcript: ENST00000426930
  gene symbol: ADAM22
  hgvsc: ENST00000426930.1:c.849-26C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381262
  ensembl transcript: ENST00000398204
  gene symbol: ADAM22
  hgvsc: ENST00000398204.4:c.2469-26C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000265727
  ensembl transcript: ENST00000265727
  gene symbol: ADAM22
  hgvsc: ENST00000265727.7:c.2577-26C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000412085
  ensembl transcript: ENST00000413139
  gene symbol: ADAM22
  hgvsc: ENST00000413139.1:c.649-26C>A
  variant of: http://identifiers.org/hgnc/201
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000008277
  ensembl protein: ENSP00000381267
  ensembl transcript: ENST00000398209
  gene symbol: ADAM22
  hgvsc: ENST00000398209.3:c.2556-26C>A
  variant of: http://identifiers.org/hgnc/201
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9686
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 1138
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5071
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37426
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1831
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.438320885912955e-5
allele num: 15532
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.254075746175069e-4
allele num: 7974
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62170
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.26e-1

FS
type: SiteQuality
SIO_000300: 4.089e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.39e1

DP
type: SiteQuality
SIO_000300: 1.581972e6

GenotypeQuality
all individuals: 39084
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1142
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5148
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1845
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5178
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9372
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.81057268722467e-5
allele num: 11350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15804
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.269e1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.897e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.604557e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.38e-1

GenotypeQuality
all individuals: 225
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5202
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1581
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5151
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 39232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.890359168241966e-4
allele num: 15870
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.612929e6

BaseQRankSum
type: SiteQuality
SIO_000300: 8.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.44e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: -3.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.26e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.76e-1

GenotypeQuality
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bin: 4.75e1
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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64764
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9610
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.189060642092747e-4
allele num: 8410
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.533e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.519e0

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.638247e6

VQSLOD
type: SiteQuality
SIO_000300: 4.69e0

MQ
type: SiteQuality
SIO_000300: 6.054e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516024377671993e-5
allele num: 65962
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.359e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.392e-1

DP
type: SiteQuality
SIO_000300: 1.659067e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.842e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

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: 51
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508750754375377e-5
allele num: 66280
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.062e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.461e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.49e-1

QD
type: SiteQuality
SIO_000300: 1.099e1

DP
type: SiteQuality
SIO_000300: 1.664605e6

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 2.047502047502048e-4
allele num: 9768
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.74e-1

FS
type: SiteQuality
SIO_000300: 3.509e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

DP
type: SiteQuality
SIO_000300: 1.669407e6

QD
type: SiteQuality
SIO_000300: 1.435e1

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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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66460
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.499766682221185e-4
allele num: 8572
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.118e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.667678e6

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: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504709741490866e-5
allele num: 66458
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.809e1

VQSLOD
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QD
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-2

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66252
num of homozygotes: 0

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

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

African
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allele frequency: 1.025851456709069e-4
allele num: 9748
num of homozygotes: 0

South Asian
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allele num: 16440
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VQSLOD
type: SiteQuality
SIO_000300: 9.87e-1

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.044277360066834e-4
allele num: 9576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64828
num of homozygotes: 0

DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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GenotypeQuality
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bin: 2.75e1
variant carriers: 29

GenotypeQuality
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bin: 4.75e1
variant carriers: 113

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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bin: 2.25e1
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GenotypeQuality
all individuals: 603
bin: 9.25e1
variant carriers: 225

GenotypeQuality
all individuals: 1355
bin: 7.75e1
variant carriers: 258

GenotypeQuality
all individuals: 19909
bin: 9.75e1
variant carriers: 15981

European (Non-Finnish)
type: Population
allele count: 6648
allele frequency: 1.029134028917304e-1
allele num: 64598
num of homozygotes: 365

South Asian
type: Population
allele count: 4619
allele frequency: 2.878599027795089e-1
allele num: 16046
num of homozygotes: 721

Other
type: Population
allele count: 146
allele frequency: 1.640449438202247e-1
allele num: 890
num of homozygotes: 17

Latino
type: Population
allele count: 3851
allele frequency: 3.394147717257183e-1
allele num: 11346
num of homozygotes: 667

African
type: Population
allele count: 941
allele frequency: 9.863731656184486e-2
allele num: 9540
num of homozygotes: 50

East Asian
type: Population
allele count: 4097
allele frequency: 4.911292256053704e-1
allele num: 8342
num of homozygotes: 1015

European (Finnish)
type: Population
allele count: 510
allele frequency: 7.81010719754977e-2
allele num: 6530
num of homozygotes: 24

VQSLOD
type: SiteQuality
SIO_000300: 6.4e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.914e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.079e-1

DP
type: SiteQuality
SIO_000300: 1.734036e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 23561
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4002
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.104144032283098e-5
allele num: 64430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9516
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.64e0

QD
type: SiteQuality
SIO_000300: 1.447e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQ
type: SiteQuality
SIO_000300: 5.934e1

FS
type: SiteQuality
SIO_000300: 6.559e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.61e-1

DP
type: SiteQuality
SIO_000300: 1.598957e6

GenotypeQuality
all individuals: 16462
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2983
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3806
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12244
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1244
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518787400139728e-5
allele num: 65842
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15188
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.394e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.156019e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.795e1

VQSLOD
type: SiteQuality
SIO_000300: -5.276e-1

GenotypeQuality
all individuals: 2995
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13047
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2962
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.614631565021828e-5
allele num: 15118
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65850
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.157989e6

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

FS
type: SiteQuality
SIO_000300: 3.136e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

QD
type: SiteQuality
SIO_000300: 1.273e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.066e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.855e0

VQSLOD
type: SiteQuality
SIO_000300: -1.77e0

GenotypeQuality
all individuals: 16510
bin: 9.75e1
variant carriers: 130

GenotypeQuality
all individuals: 611
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14510
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4519
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 116
allele frequency: 1.197604790419162e-2
allele num: 9686
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15282
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.440366972477064e-3
allele num: 872
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.339181286549708e-4
allele num: 8550
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.85203280404816e-4
allele num: 11462
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.946e0

QD
type: SiteQuality
SIO_000300: 1.328e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.28e-2

DP
type: SiteQuality
SIO_000300: 2.16532e6

GenotypeQuality
all individuals: 6824
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16522
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3011
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16436
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4527
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15360
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.177446e6

VQSLOD
type: SiteQuality
SIO_000300: 6.1e-2

FS
type: SiteQuality
SIO_000300: 3.042e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.241e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-2

GenotypeQuality
all individuals: 1160
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4538
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16688
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16436
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3738
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66030
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQRankSum
type: SiteQuality
SIO_000300: -1.16e0

FS
type: SiteQuality
SIO_000300: 1.425e0

QD
type: SiteQuality
SIO_000300: 1.501e1

VQSLOD
type: SiteQuality
SIO_000300: -2.97e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.413e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.241e0

DP
type: SiteQuality
SIO_000300: 2.178488e6

GenotypeQuality
all individuals: 63
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1904
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16923
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3737
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 4.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.483402489626556e-5
allele num: 15424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66040
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

DP
type: SiteQuality
SIO_000300: 2.179961e6

VQSLOD
type: SiteQuality
SIO_000300: -3.439e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

GenotypeQuality
all individuals: 3737
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16437
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3046
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 227
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6959
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18818
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511807214344027e-5
allele num: 66146
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.44e-1

DP
type: SiteQuality
SIO_000300: 2.200355e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

QD
type: SiteQuality
SIO_000300: 1.026e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

MQ
type: SiteQuality
SIO_000300: 5.948e1

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6962
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18968
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1909
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4550
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3736
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511441613010489e-5
allele num: 66162
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.597e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e0

DP
type: SiteQuality
SIO_000300: 2.201717e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.264e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.089e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6979
bin: 6.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2969
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3041
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9696
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.257071024512885e-4
allele num: 15910
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.4e-1

DP
type: SiteQuality
SIO_000300: 2.205815e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 5.576e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

QD
type: SiteQuality
SIO_000300: 1.028e1

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

GenotypeQuality
all individuals: 148
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
all individuals: 7
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GenotypeQuality
all individuals: 1908
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15962
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

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

African
type: Population
allele count: 6
allele frequency: 6.188118811881188e-4
allele num: 9696
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510391493475109e-5
allele num: 66208
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.6e-1

QD
type: SiteQuality
SIO_000300: 1.365e1

DP
type: SiteQuality
SIO_000300: 2.20723e6

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

GenotypeQuality
all individuals: 2966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.114711997064938e-5
allele num: 16354
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66268
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e-1

DP
type: SiteQuality
SIO_000300: 2.213636e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e0

VQSLOD
type: SiteQuality
SIO_000300: -6.9e-3

FS
type: SiteQuality
SIO_000300: 1.583e0

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

QD
type: SiteQuality
SIO_000300: 7.74e0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 16435
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 7038
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66226
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.700191404210893e-5
allele num: 11494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16362
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.65e-1

QD
type: SiteQuality
SIO_000300: 8.75e0

VQSLOD
type: SiteQuality
SIO_000300: -1.208e0

MQ
type: SiteQuality
SIO_000300: 5.682e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

DP
type: SiteQuality
SIO_000300: 2.213023e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e-1

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

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 750
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 16434
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 136
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variant carriers: 0

GenotypeQuality
all individuals: 7008
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variant carriers: 0

GenotypeQuality
all individuals: 3730
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512493193780628e-5
allele num: 66116
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.13421666053245e-5
allele num: 16302
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9610
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.781e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

DP
type: SiteQuality
SIO_000300: 2.209724e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 8.935e0

QD
type: SiteQuality
SIO_000300: 1.521e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 3035
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 128
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GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 20
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GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 16435
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.614151272220286e-4
allele num: 11476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16300
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.922e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e-1

QD
type: SiteQuality
SIO_000300: 1.236e1

FS
type: SiteQuality
SIO_000300: 4.598e0

MQRankSum
type: SiteQuality
SIO_000300: -5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.209728e6

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4520
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
all individuals: 3011
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GenotypeQuality
all individuals: 3722
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variant carriers: 0

GenotypeQuality
all individuals: 2963
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GenotypeQuality
all individuals: 92
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GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16112
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515518913676043e-5
allele num: 65984
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

QD
type: SiteQuality
SIO_000300: 1.579e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 2.199561e6

GenotypeQuality
all individuals: 17293
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
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GenotypeQuality
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GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 473
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GenotypeQuality
all individuals: 129
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 16589
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variant carriers: 307

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 275
allele frequency: 4.174129504265201e-3
allele num: 65882
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.257039169065198e-5
allele num: 15982
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.222477543346564e-4
allele num: 9574
num of homozygotes: 0

Latino
type: Population
allele count: 24
allele frequency: 2.09643605870021e-3
allele num: 11448
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.138952164009112e-3
allele num: 878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.548211036992117e-4
allele num: 6596
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

FS
type: SiteQuality
SIO_000300: 6.929999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e0

QD
type: SiteQuality
SIO_000300: 1.447e1

MQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

DP
type: SiteQuality
SIO_000300: 2.192376e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1085
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variant carriers: 0

GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 243
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GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 2932
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GenotypeQuality
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GenotypeQuality
all individuals: 1878
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1914
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GenotypeQuality
all individuals: 4417
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65742
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.744316194473592e-5
allele num: 11436
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 6.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.57e-1

QD
type: SiteQuality
SIO_000300: 6.99e0

VQSLOD
type: SiteQuality
SIO_000300: -1.023e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

DP
type: SiteQuality
SIO_000300: 2.170004e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16330
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2928
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14164
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65664
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15742
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.049538203190596e-4
allele num: 9528
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

VQSLOD
type: SiteQuality
SIO_000300: -2.643e-1

DP
type: SiteQuality
SIO_000300: 2.151019e6

FS
type: SiteQuality
SIO_000300: 6.343e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.577e0

QD
type: SiteQuality
SIO_000300: 1.412e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.49e-1

GenotypeQuality
all individuals: 2156
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2925
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.354047528275512e-5
allele num: 15738
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.74e-1

DP
type: SiteQuality
SIO_000300: 2.148351e6

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.073e0

QD
type: SiteQuality
SIO_000300: 1.16e1

FS
type: SiteQuality
SIO_000300: 1.715e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

GenotypeQuality
all individuals: 2919
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1355
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
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variant carriers: 0

GenotypeQuality
all individuals: 3623
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16323
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2801
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9506
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.626834253637999e-5
allele num: 65558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.125548e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.457e1

GenotypeQuality
all individuals: 1860
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2770
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2914
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2593
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1533
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variant carriers: 0

GenotypeQuality
all individuals: 4872
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variant carriers: 0

GenotypeQuality
all individuals: 1943
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variant carriers: 0

GenotypeQuality
all individuals: 2130
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variant carriers: 0

GenotypeQuality
all individuals: 7807
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variant carriers: 0

GenotypeQuality
all individuals: 16317
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65266
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.48760866744518e-5
allele num: 15414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.229e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.100221e6

FS
type: SiteQuality
SIO_000300: 8.694000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.039e-1

QD
type: SiteQuality
SIO_000300: 1.551e1

GenotypeQuality
all individuals: 248
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 79
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 881
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variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.984725965858042e-4
allele num: 2226
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.367003367003367e-4
allele num: 2970
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.470000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.64e-2

FS
type: SiteQuality
SIO_000300: 1.335e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.871e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.04916e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

GenotypeQuality
all individuals: 185
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 173
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3934
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.685772083614295e-4
allele num: 5932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3254
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.399e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.691e0

DP
type: SiteQuality
SIO_000300: 1.52886e5

VQSLOD
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.112e0

MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-2

QD
type: SiteQuality
SIO_000300: 9.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

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

GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4107
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.990430622009569e-4
allele num: 3344
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.55976e5

MQRankSum
type: SiteQuality
SIO_000300: -3.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

FS
type: SiteQuality
SIO_000300: 1.079e0

VQSLOD
type: SiteQuality
SIO_000300: -1.863e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.117e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 1.135e1

GenotypeQuality
all individuals: 193
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1502
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.611863313990974e-4
allele num: 6204
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3360
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.966e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

DP
type: SiteQuality
SIO_000300: 1.56861e5

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 8

GenotypeQuality
all individuals: 2312
bin: 9.75e1
variant carriers: 2216

GenotypeQuality
all individuals: 145
bin: 7.75e1
variant carriers: 43

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 104
bin: 8.25e1
variant carriers: 40

GenotypeQuality
all individuals: 367
bin: 6.75e1
variant carriers: 31

GenotypeQuality
all individuals: 3381
bin: 6.25e1
variant carriers: 34

GenotypeQuality
all individuals: 138
bin: 7.25e1
variant carriers: 16

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 26

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 11

European (Finnish)
type: Population
allele count: 129
allele frequency: 8.17490494296578e-2
allele num: 1578
num of homozygotes: 2

Latino
type: Population
allele count: 40
allele frequency: 2.150537634408602e-1
allele num: 186
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 501
allele frequency: 1.36437908496732e-1
allele num: 3672
num of homozygotes: 30

African
type: Population
allele count: 28
allele frequency: 5.035971223021583e-2
allele num: 556
num of homozygotes: 1

South Asian
type: Population
allele count: 2010
allele frequency: 2.777010223818734e-1
allele num: 7238
num of homozygotes: 298

Other
type: Population
allele count: 35
allele frequency: 1.944444444444444e-1
allele num: 180
num of homozygotes: 5

East Asian
type: Population
allele count: 89
allele frequency: 4.494949494949495e-1
allele num: 198
num of homozygotes: 16

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-2

FS
type: SiteQuality
SIO_000300: 5.35e-1

QD
type: SiteQuality
SIO_000300: 1.361e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.827e0

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

DP
type: SiteQuality
SIO_000300: 1.90828e5

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 655
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 128
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 93
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.422993492407809e-4
allele num: 3688
num of homozygotes: 0

Other
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: 556
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.94e0

QD
type: SiteQuality
SIO_000300: 1.678e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

DP
type: SiteQuality
SIO_000300: 1.75836e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5222
bin: 6.25e1
variant carriers: 0

Latino
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: 7298
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.792114695340502e-3
allele num: 558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3696
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 1.765e5

QD
type: SiteQuality
SIO_000300: 1.182e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.176e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.416e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.77e-2

FS
type: SiteQuality
SIO_000300: 1.119e0

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

GenotypeQuality
all individuals: 126
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1059
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1278
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5084
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: 3.50385423966363e-4
allele num: 2854
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

DP
type: SiteQuality
SIO_000300: 1.1384e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.55e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

QD
type: SiteQuality
SIO_000300: 5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.680999999999999e0

FS
type: SiteQuality
SIO_000300: 4.1298e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.166e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 158
bin: 8.25e1
variant carriers: 103

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 61

GenotypeQuality
all individuals: 1169
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 85
bin: 9.25e1
variant carriers: 57

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 101

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 34

GenotypeQuality
all individuals: 192
bin: 4.75e1
variant carriers: 60

GenotypeQuality
all individuals: 182
bin: 6.25e1
variant carriers: 14

GenotypeQuality
all individuals: 415
bin: 1.25e1
variant carriers: 57

GenotypeQuality
all individuals: 1454
bin: 2.25e1
variant carriers: 122

Other
type: Population
allele count: 19
allele frequency: 1.727272727272727e-1
allele num: 110
num of homozygotes: 2

South Asian
type: Population
allele count: 849
allele frequency: 2.683312262958281e-1
allele num: 3164
num of homozygotes: 126

African
type: Population
allele count: 56
allele frequency: 1.186440677966102e-1
allele num: 472
num of homozygotes: 2

East Asian
type: Population
allele count: 77
allele frequency: 4.529411764705882e-1
allele num: 170
num of homozygotes: 16

Latino
type: Population
allele count: 32
allele frequency: 2.424242424242424e-1
allele num: 132
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 104
allele frequency: 7.975460122699386e-2
allele num: 1304
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 258
allele frequency: 1.180237877401647e-1
allele num: 2186
num of homozygotes: 12

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.5995e4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

QD
type: SiteQuality
SIO_000300: 1.701e1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.69e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 37457
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10457
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.997361161089121e-5
allele num: 66696
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.272e0

DP
type: SiteQuality
SIO_000300: 1.940596e6

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.498e1

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4111
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 822
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2695
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10453
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.449e0

DP
type: SiteQuality
SIO_000300: 1.940693e6

VQSLOD
type: SiteQuality
SIO_000300: -1.633e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.34e-1

FS
type: SiteQuality
SIO_000300: 3.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.33e-1

MQ
type: SiteQuality
SIO_000300: 5.892e1

QD
type: SiteQuality
SIO_000300: 1.29e1

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4108
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 7.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.552e1

FS
type: SiteQuality
SIO_000300: 1.4459e1

MQRankSum
type: SiteQuality
SIO_000300: 8.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.25e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.122e0

DP
type: SiteQuality
SIO_000300: 1.940777e6

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37533
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 822
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4110
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2697
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.515e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.940716e6

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4105
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2693
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37666
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.993344924755681e-5
allele num: 66716
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

MQRankSum
type: SiteQuality
SIO_000300: -1.83e-1

DP
type: SiteQuality
SIO_000300: 1.941759e6

FS
type: SiteQuality
SIO_000300: 2.515e0

QD
type: SiteQuality
SIO_000300: 1.421e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.69e-1

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37668
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4100
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997691777331455e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.941208e6

FS
type: SiteQuality
SIO_000300: 5.29e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.111e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.320000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.051e1

GenotypeQuality
all individuals: 4100
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2694
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37668
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10454
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

African
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: 66718
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.320000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.111e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.941208e6

QD
type: SiteQuality
SIO_000300: 1.051e1

GenotypeQuality
all individuals: 1482
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2510
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37669
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2693
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.199076710932582e-4
allele num: 66718
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.79e-1

DP
type: SiteQuality
SIO_000300: 1.941409e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

QD
type: SiteQuality
SIO_000300: 1.116e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.28e-1

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.127e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

DP
type: SiteQuality
SIO_000300: 1.940833e6

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 1.092e1

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

GenotypeQuality
all individuals: 37679
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.245e1

MQRankSum
type: SiteQuality
SIO_000300: -6.61e-1

DP
type: SiteQuality
SIO_000300: 1.940846e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.25e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 9.320000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

FS
type: SiteQuality
SIO_000300: 3.248e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e-1

GenotypeQuality
all individuals: 1482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
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variant carriers: 0

GenotypeQuality
all individuals: 4087
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

VQSLOD
type: SiteQuality
SIO_000300: 1.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 6.738e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

DP
type: SiteQuality
SIO_000300: 1.940778e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37687
bin: 6.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

FS
type: SiteQuality
SIO_000300: 7.576e0

DP
type: SiteQuality
SIO_000300: 1.940789e6

QD
type: SiteQuality
SIO_000300: 1.166e1

GenotypeQuality
all individuals: 821
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.85e0

VQSLOD
type: SiteQuality
SIO_000300: 6.56e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

FS
type: SiteQuality
SIO_000300: 5.194e0

ClippingRankSum
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SIO_000300: -2.47e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.619e0

QD
type: SiteQuality
SIO_000300: 1.129e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

DP
type: SiteQuality
SIO_000300: 1.940717e6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.940663e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-2

BaseQRankSum
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.75e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.382e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e-1

DP
type: SiteQuality
SIO_000300: 1.940541e6

QD
type: SiteQuality
SIO_000300: 1.199e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.103e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.365e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.02e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.912e1

VQSLOD
type: SiteQuality
SIO_000300: -5.51e-1

DP
type: SiteQuality
SIO_000300: 1.940421e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.38e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

FS
type: SiteQuality
SIO_000300: 1.843e0

MQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

DP
type: SiteQuality
SIO_000300: 1.939335e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.06e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4079
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.409e0

DP
type: SiteQuality
SIO_000300: 1.938476e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

QD
type: SiteQuality
SIO_000300: 9.75e0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4079
bin: 9.75e1
variant carriers: 27

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2498
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2691
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1480
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.552705868220313e-4
allele num: 66596
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.021867974657674e-4
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.793557325943886e-4
allele num: 11548
num of homozygotes: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 1.937526e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.08e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.801e0

FS
type: SiteQuality
SIO_000300: 2.894e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

QD
type: SiteQuality
SIO_000300: 1.289e1

GenotypeQuality
all individuals: 4043
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9654
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.179245283018868e-4
allele num: 8480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.938e0

QD
type: SiteQuality
SIO_000300: 9.220000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.423e0

MQ
type: SiteQuality
SIO_000300: 5.888e1

FS
type: SiteQuality
SIO_000300: 8.956e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

DP
type: SiteQuality
SIO_000300: 1.892322e6

VQSLOD
type: SiteQuality
SIO_000300: -2.751e0

GenotypeQuality
all individuals: 804
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35769
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4041
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526298116548124e-5
allele num: 65518
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.535e0

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

DP
type: SiteQuality
SIO_000300: 1.875566e6

QD
type: SiteQuality
SIO_000300: 8.859999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 5.716e1

GenotypeQuality
all individuals: 426
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4039
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2212
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2420
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64692
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.052188552188552e-4
allele num: 9504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.154e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

DP
type: SiteQuality
SIO_000300: 1.802661e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

QD
type: SiteQuality
SIO_000300: 2.713e1

VQSLOD
type: SiteQuality
SIO_000300: -2.688e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.855e1

GenotypeQuality
all individuals: 8886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4038
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 33229
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3744
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.128201985537444e-5
allele num: 16318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8274
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.818342151675486e-5
allele num: 11340
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.789795e6

VQSLOD
type: SiteQuality
SIO_000300: -1.235e0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

FS
type: SiteQuality
SIO_000300: 1.368e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQ
type: SiteQuality
SIO_000300: 5.861e1

QD
type: SiteQuality
SIO_000300: 1.633e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 2422
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2286
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1619
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5346
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15982
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.093374152635032e-4
allele num: 9146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11170
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.432747e6

MQRankSum
type: SiteQuality
SIO_000300: -3.916e0

QD
type: SiteQuality
SIO_000300: 5.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.795e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.473e0

MQ
type: SiteQuality
SIO_000300: 5.678e1

GenotypeQuality
all individuals: 11368
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4027
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3804
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2299
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61144
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.81257930034439e-4
allele num: 11034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15758
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.085e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

QD
type: SiteQuality
SIO_000300: 9.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.363551e6

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

GenotypeQuality
all individuals: 152
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38959
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2545
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9588
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66592
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.216249087813184e-4
allele num: 16444
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.385e0

QD
type: SiteQuality
SIO_000300: 1.216e1

DP
type: SiteQuality
SIO_000300: 1.732572e6

MQRankSum
type: SiteQuality
SIO_000300: 2.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.49e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.13e-1

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1375
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9591
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.021867974657674e-4
allele num: 9786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.061e0

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

FS
type: SiteQuality
SIO_000300: 6.058e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.118e-1

DP
type: SiteQuality
SIO_000300: 1.734575e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
all individuals: 621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39657
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.737948e6

VQSLOD
type: SiteQuality
SIO_000300: 3.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.965e0

FS
type: SiteQuality
SIO_000300: 1.059e0

MQ
type: SiteQuality
SIO_000300: 5.909e1

QD
type: SiteQuality
SIO_000300: 1.332e1

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0