2-98744734-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744734
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744734
    reference: chr 2
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.119T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6813T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.941T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.735T>A
  hgvsp: ENSP00000417955.1:p.Asp245Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.285T>A
  hgvsp: ENSP00000389463.2:p.Asp95Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5553T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.735T>A
  hgvsp: ENSP00000411168.1:p.Asp245Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*422T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.735T>A
  hgvsp: ENSP00000401959.1:p.Asp245Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.735T>A
  hgvsp: ENSP00000388158.1:p.Asp245Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*109T>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22469
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp245Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

2-98744740-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744740
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744740
    reference: chr 2
allele count: 84
allele frequency: 6.956521739130435e-4
allele num: 120750
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.741T>C
  hgvsp: ENST00000477737.1:c.741T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*428T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.125T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.741T>C
  hgvsp: ENST00000435344.1:c.741T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.291T>C
  hgvsp: ENST00000451075.2:c.291T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6819T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.741T>C
  hgvsp: ENST00000433678.1:c.741T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.741T>C
  hgvsp: ENST00000416277.1:c.741T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.947T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*115T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5547T>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 9.75e1
  variant carriers: 73
genotype quality: GenotypeQuality
hgvs: p.Pro247Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-98744753-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744753
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744753
    reference: chr 2
allele count: 6
allele frequency: 4.968368056705641e-5
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.754G>T
  hgvsp: ENSP00000417955.1:p.Glu252Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.138G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.304G>T
  hgvsp: ENSP00000389463.2:p.Glu102Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*441G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*128G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5534G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6832G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.754G>T
  hgvsp: ENSP00000411168.1:p.Glu252Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.754G>T
  hgvsp: ENSP00000388158.1:p.Glu252Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.754G>T
  hgvsp: ENSP00000401959.1:p.Glu252Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.960G>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15451
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu252Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

2-98744784-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744784
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744784
    reference: chr 2
allele count: 4
allele frequency: 3.312300226892566e-5
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.991C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5503C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.785C>T
  hgvsp: ENSP00000401959.1:p.Pro262Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.785C>T
  hgvsp: ENSP00000411168.1:p.Pro262Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.785C>T
  hgvsp: ENSP00000417955.1:p.Pro262Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*159C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.335C>T
  hgvsp: ENSP00000389463.2:p.Pro112Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6863C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*472C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.785C>T
  hgvsp: ENSP00000388158.1:p.Pro262Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.169C>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro262Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

2-98744785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744785
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744785
    reference: chr 2
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*473G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.786G>A
  hgvsp: ENST00000433678.1:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.786G>A
  hgvsp: ENST00000435344.1:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.336G>A
  hgvsp: ENST00000451075.2:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.992G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.786G>A
  hgvsp: ENST00000416277.1:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*160G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6864G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.786G>A
  hgvsp: ENST00000477737.1:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.170G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5502G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro262Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

2-98744802-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744802
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744802
    reference: chr 2
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.803T>A
  hgvsp: ENSP00000401959.1:p.Val268Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.803T>A
  hgvsp: ENSP00000388158.1:p.Val268Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*490T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1009T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.353T>A
  hgvsp: ENSP00000389463.2:p.Val118Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.803T>A
  hgvsp: ENSP00000411168.1:p.Val268Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.803T>A
  hgvsp: ENSP00000417955.1:p.Val268Glu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.187T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6881T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5485T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*177T>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15444
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val268Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

2-98744802-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744802
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744802
    reference: chr 2
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6881T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1009T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5485T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.803T>C
  hgvsp: ENSP00000388158.1:p.Val268Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.803T>C
  hgvsp: ENSP00000417955.1:p.Val268Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.803T>C
  hgvsp: ENSP00000411168.1:p.Val268Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*177T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.803T>C
  hgvsp: ENSP00000401959.1:p.Val268Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*490T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.353T>C
  hgvsp: ENSP00000389463.2:p.Val118Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.187T>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2672
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val268Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

2-98744812-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744812
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744812
    reference: chr 2
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*187C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6891C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.813C>G
  hgvsp: ENSP00000417955.1:p.Asn271Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.813C>G
  hgvsp: ENSP00000401959.1:p.Asn271Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5475C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.813C>G
  hgvsp: ENSP00000411168.1:p.Asn271Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.813C>G
  hgvsp: ENSP00000388158.1:p.Asn271Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1019C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.197C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.363C>G
  hgvsp: ENSP00000389463.2:p.Asn121Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*500C>G
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn271Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

2-98744812-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744812
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744812
    reference: chr 2
allele count: 14
allele frequency: 1.159305079412398e-4
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5475C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1019C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.813C>T
  hgvsp: ENST00000416277.1:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6891C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.363C>T
  hgvsp: ENST00000451075.2:c.363C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.813C>T
  hgvsp: ENST00000477737.1:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.813C>T
  hgvsp: ENST00000433678.1:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*187C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.813C>T
  hgvsp: ENST00000435344.1:c.813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.197C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*500C>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn271Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

2-98744826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744826
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744826
    reference: chr 2
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.377G>A
  hgvsp: ENSP00000389463.2:p.Gly126Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.827G>A
  hgvsp: ENSP00000411168.1:p.Gly276Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6905G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.827G>A
  hgvsp: ENSP00000417955.1:p.Gly276Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.211G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.827G>A
  hgvsp: ENSP00000401959.1:p.Gly276Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.827G>A
  hgvsp: ENSP00000388158.1:p.Gly276Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*201G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*514G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1033G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5461G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly276Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP

2-98744832-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744832
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744832
    reference: chr 2
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.833T>C
  hgvsp: ENSP00000401959.1:p.Ile278Thr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.833T>C
  hgvsp: ENSP00000388158.1:p.Ile278Thr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5455T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*207T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.383T>C
  hgvsp: ENSP00000389463.2:p.Ile128Thr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.833T>C
  hgvsp: ENSP00000417955.1:p.Ile278Thr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6911T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.833T>C
  hgvsp: ENSP00000411168.1:p.Ile278Thr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1039T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*520T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.217T>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile278Thr
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

2-98744834-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744834
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744834
    reference: chr 2
allele count: 2
allele frequency: 1.656863557286057e-5
allele num: 120710
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.385G>C
  hgvsp: ENSP00000389463.2:p.Ala129Pro
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.219G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.835G>C
  hgvsp: ENSP00000401959.1:p.Ala279Pro
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.835G>C
  hgvsp: ENSP00000411168.1:p.Ala279Pro
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.835G>C
  hgvsp: ENSP00000388158.1:p.Ala279Pro
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5453G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1041G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6913G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*209G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.835G>C
  hgvsp: ENSP00000417955.1:p.Ala279Pro
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*522G>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala279Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

2-98744836-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744836
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744836
    reference: chr 2
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.837T>C
  hgvsp: ENST00000477737.1:c.837T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*524T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.837T>C
  hgvsp: ENST00000416277.1:c.837T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5451T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.837T>C
  hgvsp: ENST00000435344.1:c.837T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.387T>C
  hgvsp: ENST00000451075.2:c.387T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.837T>C
  hgvsp: ENST00000433678.1:c.837T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6915T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*211T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1043T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.221T>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala279Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

2-98744840-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744840
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744840
    reference: chr 2
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5447C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.225C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.841C>G
  hgvsp: ENSP00000417955.1:p.Leu281Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*528C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.841C>G
  hgvsp: ENSP00000411168.1:p.Leu281Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1047C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.841C>G
  hgvsp: ENSP00000401959.1:p.Leu281Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.841C>G
  hgvsp: ENSP00000388158.1:p.Leu281Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*215C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.391C>G
  hgvsp: ENSP00000389463.2:p.Leu131Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6919C>G
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu281Val
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

2-98744844-AGGATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744844
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744838
    reference: chr 2
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.231_236delGATCTG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.847_852delGATCTG
  hgvsp: ENSP00000388158.1:p.Asp283_Leu284del
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1053_1058delGATCTG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.847_852delGATCTG
  hgvsp: ENSP00000401959.1:p.Asp283_Leu284del
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.847_852delGATCTG
  hgvsp: ENSP00000411168.1:p.Asp283_Leu284del
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*221_*226delGATCTG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.397_402delGATCTG
  hgvsp: ENSP00000389463.2:p.Asp133_Leu134del
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*534_*539delGATCTG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.847_852delGATCTG
  hgvsp: ENSP00000417955.1:p.Asp283_Leu284del
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp283_Leu284del
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: AGGATCT
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

2-98744860-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744860
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744860
    reference: chr 2
allele count: 2
allele frequency: 1.658154805332626e-5
allele num: 120616
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.861G>A
  hgvsp: ENST00000416277.1:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5427G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1067G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.861G>A
  hgvsp: ENST00000477737.1:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.861G>A
  hgvsp: ENST00000433678.1:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.411G>A
  hgvsp: ENST00000451075.2:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.861G>A
  hgvsp: ENST00000435344.1:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*235G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*548G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.245G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6939G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys287Lys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

2-98744875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744875
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744875
    reference: chr 2
allele count: 1
allele frequency: 8.303165166561494e-6
allele num: 120436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+4G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+4G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+4G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+4G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+4G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6954G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+4G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5412G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+4G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+4G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+4G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.872+4G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

2-98744876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744876
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744876
    reference: chr 2
allele count: 4
allele frequency: 3.321597023849066e-5
allele num: 120424
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+5G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+5G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+5G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+5G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+5G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+5G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6955G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+5G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+5G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+5G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5411G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7524
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15220
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.872+5G>A
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-98744878-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744878
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744878
    reference: chr 2
allele count: 1
allele frequency: 8.306199747491528e-6
allele num: 120392
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+7A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+7A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+7A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+7A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+7A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+7A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+7A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6957A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+7A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5409A>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+7A>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.872+7A>C
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

2-98744882-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744882
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744882
    reference: chr 2
allele count: 1
allele frequency: 8.313934153641504e-6
allele num: 120280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+11A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+11A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+11A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+11A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+11A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+11A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5405A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+11A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+11A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+11A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6961A>G
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

2-98744887-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744887
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744887
    reference: chr 2
allele count: 1
allele frequency: 8.328336331534413e-6
allele num: 120072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+16G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+16G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6966G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+16G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+16G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5400G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+16G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+16G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+16G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+16G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+16G>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

2-98744891-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744891
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744891
    reference: chr 2
allele count: 1
allele frequency: 8.335973058135075e-6
allele num: 119962
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+20T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+20T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+20T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+20T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+20T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+20T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6970T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+20T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+20T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+20T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5396T>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14788
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

2-98744893-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744893
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744893
    reference: chr 2
allele count: 2
allele frequency: 1.668335001668335e-5
allele num: 119880
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+22G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+22G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5394G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+22G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+22G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+22G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6972G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+22G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+22G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+22G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+22G>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

2-98744905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744905
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744905
    reference: chr 2
allele count: 12
allele frequency: 1.004570797126927e-4
allele num: 119454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+34G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5382G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+34G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+34G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+34G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+34G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+34G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+34G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+34G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6984G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+34G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12372
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18116
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

2-98744906-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744906
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744906
    reference: chr 2
allele count: 4
allele frequency: 3.35677481076182e-5
allele num: 119162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+35C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+35C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6985C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+35C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+35C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+35C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+35C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5381C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+35C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+35C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+35C>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11954
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17326
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

2-98744907-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744907
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744907
    reference: chr 2
allele count: 5
allele frequency: 4.194701253376734e-5
allele num: 119198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+36G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+36G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+36G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+36G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+36G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+36G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+36G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5380G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+36G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+36G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6986G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

2-98744907-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744907
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744907
    reference: chr 2
allele count: 2
allele frequency: 1.677880501350694e-5
allele num: 119198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+36G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+36G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+36G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5380G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+36G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+36G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+36G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+36G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6986G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+36G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+36G>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16927
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

2-98744913-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744913
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744913
    reference: chr 2
allele count: 1
allele frequency: 8.424883736604435e-6
allele num: 118696
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+42C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+42C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+42C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+42C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+42C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+42C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+42C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+42C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+42C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6992C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5374C>G
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10081
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

2-98744915-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744915
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744915
    reference: chr 2
allele count: 1090
allele frequency: 9.182349670614796e-3
allele num: 118706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+44T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+44T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6994T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5372T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+44T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+44T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+44T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+44T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+44T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+44T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+44T>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8512
  bin: 2.25e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 13144
  bin: 2.75e1
  variant carriers: 213
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9569
  bin: 3.25e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 3.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 4.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 4.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 10064
  bin: 1.75e1
  variant carriers: 96
genotype quality: GenotypeQuality
num of homozygotes: 5
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

2-98744916-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744916
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744916
    reference: chr 2
allele count: 1
allele frequency: 8.439103429651633e-6
allele num: 118496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+45G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+45G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+45G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+45G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+45G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+45G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5371G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+45G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+6995G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+45G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+45G>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9040
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

2-98744922-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98744922
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98744922
    reference: chr 2
allele count: 1
allele frequency: 8.513536523071684e-6
allele num: 117460
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.422+51A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1078+51A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.256+51A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+7001A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*559+51A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.872+51A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*246+51A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.872+51A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.872+51A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.872+51A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-5365A>G
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12698
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9982
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

2-98750236-GCACGGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750236
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750230
    reference: chr 2
allele count: 2
allele frequency: 1.663838141825563e-5
allele num: 120204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*247-47_*247-42delGGACAC
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.873-47_873-42delGGACAC
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.423-47_423-42delGGACAC
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1079-47_1079-42delGGACAC
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-47_503-42delGGACAC
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.873-47_873-42delGGACAC
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.873-47_873-42delGGACAC
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.352_357delGGACAC
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.873-47_873-42delGGACAC
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*560-47_*560-42delGGACAC
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: GCACGGA
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

2-98750239-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750239
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750239
    reference: chr 2
allele count: 2
allele frequency: 1.66616681662168e-5
allele num: 120036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*247-48C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*560-48C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12318C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-48C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.873-48C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.873-48C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.351C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1079-48C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.873-48C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.423-48C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.873-48C>T
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-98750240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750240
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750240
    reference: chr 2
allele count: 93
allele frequency: 7.737104825291182e-4
allele num: 120200
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.873-47G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1079-47G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.873-47G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*247-47G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.352G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.423-47G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-47G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*560-47G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.873-47G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.873-47G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12319G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8210
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 9.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7330
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP

2-98750249-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750249
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750249
    reference: chr 2
allele count: 1
allele frequency: 8.314348903337379e-6
allele num: 120274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1079-38C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*560-38C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*247-38C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.873-38C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.873-38C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-38C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12328C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.423-38C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.873-38C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.361C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.873-38C>T
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

2-98750250-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750250
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750250
    reference: chr 2
allele count: 1
allele frequency: 8.310065150910783e-6
allele num: 120336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1079-37G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12329G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.873-37G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-37G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.362G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.873-37G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.873-37G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.423-37G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*560-37G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*247-37G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.873-37G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

2-98750250-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750250
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750250
    reference: chr 2
allele count: 1
allele frequency: 8.310065150910783e-6
allele num: 120336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*247-37G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-37G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.873-37G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.873-37G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12329G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.873-37G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1079-37G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.423-37G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.362G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.873-37G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*560-37G>C
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

2-98750268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750268
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750268
    reference: chr 2
allele count: 1
allele frequency: 8.291048983517394e-6
allele num: 120612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.873-19G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*247-19G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.873-19G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*560-19G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.873-19G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.423-19G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.380G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12347G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.873-19G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1079-19G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-19G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

2-98750275-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750275
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750275
    reference: chr 2
allele count: 1
allele frequency: 8.286789200656313e-6
allele num: 120674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*247-12T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.423-12T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.873-12T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.873-12T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1079-12T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*560-12T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.387T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.873-12T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-12T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.873-12T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12354T>C
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6306
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

2-98750280-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750280
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750280
    reference: chr 2
allele count: 6
allele frequency: 4.970425965505244e-5
allele num: 120714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.503-7G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*247-7G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1079-7G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.873-7G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.392G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.423-7G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.873-7G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.873-7G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.873-7G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12359G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*560-7G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.873-7G>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

2-98750293-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750293
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750293
    reference: chr 2
allele count: 28
allele frequency: 2.318878987643688e-4
allele num: 120748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.879C>T
  hgvsp: ENST00000435344.1:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12372C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*566C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1085C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.429C>T
  hgvsp: ENST00000451075.2:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.879C>T
  hgvsp: ENST00000433678.1:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.879C>T
  hgvsp: ENST00000477737.1:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.405C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.879C>T
  hgvsp: ENST00000416277.1:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.509C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*253C>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His293His
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

2-98750302-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750302
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750302
    reference: chr 2
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*575C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.414C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.888C>G
  hgvsp: ENST00000433678.1:c.888C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.888C>G
  hgvsp: ENST00000416277.1:c.888C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.888C>G
  hgvsp: ENST00000477737.1:c.888C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.518C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.888C>G
  hgvsp: ENST00000435344.1:c.888C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12381C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1094C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*262C>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.438C>G
  hgvsp: ENST00000451075.2:c.438C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala296Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

2-98750303-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750303
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750303
    reference: chr 2
allele count: 178
allele frequency: 1.473924780153354e-3
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.439G>A
  hgvsp: ENSP00000389463.2:p.Glu147Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12382G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.889G>A
  hgvsp: ENSP00000417955.1:p.Glu297Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.889G>A
  hgvsp: ENSP00000388158.1:p.Glu297Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1095G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.519G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.889G>A
  hgvsp: ENSP00000411168.1:p.Glu297Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*263G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.889G>A
  hgvsp: ENSP00000401959.1:p.Glu297Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.415G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*576G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7349
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 9.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: p.Glu297Lys
num of homozygotes: 4
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

2-98750303-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750303
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750303
    reference: chr 2
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.415G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.889G>T
  hgvsp: ENSP00000401959.1:p.Glu297Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.439G>T
  hgvsp: ENSP00000389463.2:p.Glu147Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12382G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*576G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.889G>T
  hgvsp: ENSP00000411168.1:p.Glu297Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1095G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.519G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.889G>T
  hgvsp: ENSP00000388158.1:p.Glu297Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.889G>T
  hgvsp: ENSP00000417955.1:p.Glu297Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*263G>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu297Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

2-98750307-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750307
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750307
    reference: chr 2
allele count: 3
allele frequency: 2.484019474712682e-5
allele num: 120772
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.893G>A
  hgvsp: ENSP00000417955.1:p.Arg298Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.443G>A
  hgvsp: ENSP00000389463.2:p.Arg148Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.523G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.893G>A
  hgvsp: ENSP00000411168.1:p.Arg298Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*267G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.893G>A
  hgvsp: ENSP00000401959.1:p.Arg298Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12386G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*580G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.893G>A
  hgvsp: ENSP00000388158.1:p.Arg298Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.419G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1099G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Arg298Lys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

2-98750310-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750310
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750308
    reference: chr 2
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1105_1106delAG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.449_450delAG
  hgvsp: ENSP00000389463.2:p.Glu150ValfsTer13
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.899_900delAG
  hgvsp: ENSP00000401959.1:p.Glu300ValfsTer13
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.425_426delAG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.899_900delAG
  hgvsp: ENSP00000411168.1:p.Glu300ValfsTer13
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.899_900delAG
  hgvsp: ENSP00000388158.1:p.Glu300ValfsTer13
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*586_*587delAG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*273_*274delAG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.529_530delAG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.899_900delAG
  hgvsp: ENSP00000417955.1:p.Glu300ValfsTer13
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12392_702+12393delAG
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu300ValfsTer13
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: CAG
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-98750327-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750327
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750327
    reference: chr 2
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1119C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.439C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.913C>T
  hgvsp: ENSP00000417955.1:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.913C>T
  hgvsp: ENSP00000411168.1:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.913C>T
  hgvsp: ENSP00000401959.1:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.913C>T
  hgvsp: ENSP00000388158.1:p.Pro305Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12406C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.543C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*600C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.463C>T
  hgvsp: ENSP00000389463.2:p.Pro155Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*287C>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro305Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

2-98750331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750331
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750331
    reference: chr 2
allele count: 1
allele frequency: 8.279790686891435e-6
allele num: 120776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.547C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.917C>T
  hgvsp: ENSP00000417955.1:p.Ala306Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.917C>T
  hgvsp: ENSP00000388158.1:p.Ala306Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.917C>T
  hgvsp: ENSP00000411168.1:p.Ala306Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.467C>T
  hgvsp: ENSP00000389463.2:p.Ala156Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.917C>T
  hgvsp: ENSP00000401959.1:p.Ala306Val
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1123C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*291C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*604C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.443C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12410C>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala306Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

2-98750332-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750332
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750332
    reference: chr 2
allele count: 1
allele frequency: 8.279790686891435e-6
allele num: 120776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1124A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.468A>G
  hgvsp: ENST00000451075.2:c.468A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.918A>G
  hgvsp: ENST00000435344.1:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.918A>G
  hgvsp: ENST00000416277.1:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.918A>G
  hgvsp: ENST00000477737.1:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*605A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*292A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12411A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.444A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.548A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.918A>G
  hgvsp: ENST00000433678.1:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala306Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-98750335-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750335
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750335
    reference: chr 2
allele count: 1
allele frequency: 8.280064915708939e-6
allele num: 120772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.921C>A
  hgvsp: ENSP00000388158.1:p.Phe307Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12414C>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.921C>A
  hgvsp: ENSP00000401959.1:p.Phe307Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.921C>A
  hgvsp: ENSP00000411168.1:p.Phe307Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.921C>A
  hgvsp: ENSP00000417955.1:p.Phe307Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.551C>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*608C>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.471C>A
  hgvsp: ENSP00000389463.2:p.Phe157Leu
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1127C>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*295C>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.447C>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Phe307Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

2-98750344-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750344
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750344
    reference: chr 2
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*617G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*304G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.560G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12423G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.480G>T
  hgvsp: ENSP00000389463.2:p.Lys160Asn
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.930G>T
  hgvsp: ENSP00000401959.1:p.Lys310Asn
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.930G>T
  hgvsp: ENSP00000388158.1:p.Lys310Asn
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.930G>T
  hgvsp: ENSP00000411168.1:p.Lys310Asn
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.930G>T
  hgvsp: ENSP00000417955.1:p.Lys310Asn
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1136G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.456G>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys310Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

2-98750345-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750345
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750345
    reference: chr 2
allele count: 4
allele frequency: 3.311971119611837e-5
allele num: 120774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.931G>T
  hgvsp: ENSP00000388158.1:p.Asp311Tyr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.931G>T
  hgvsp: ENSP00000401959.1:p.Asp311Tyr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1137G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.931G>T
  hgvsp: ENSP00000417955.1:p.Asp311Tyr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.481G>T
  hgvsp: ENSP00000389463.2:p.Asp161Tyr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.931G>T
  hgvsp: ENSP00000411168.1:p.Asp311Tyr
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*305G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.561G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*618G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12424G>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.457G>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp311Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

2-98750354-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750354
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750354
    reference: chr 2
allele count: 5
allele frequency: 4.14003245785447e-5
allele num: 120772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.490A>G
  hgvsp: ENSP00000389463.2:p.Asn164Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.940A>G
  hgvsp: ENSP00000401959.1:p.Asn314Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12433A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*627A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.940A>G
  hgvsp: ENSP00000388158.1:p.Asn314Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*314A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.570A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.466A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.940A>G
  hgvsp: ENSP00000417955.1:p.Asn314Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.940A>G
  hgvsp: ENSP00000411168.1:p.Asn314Asp
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1146A>G
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn314Asp
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

2-98750358-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750358
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750358
    reference: chr 2
allele count: 5
allele frequency: 4.14003245785447e-5
allele num: 120772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.944T>C
  hgvsp: ENSP00000388158.1:p.Val315Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.944T>C
  hgvsp: ENSP00000417955.1:p.Val315Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.494T>C
  hgvsp: ENSP00000389463.2:p.Val165Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000448079
  gene symbol: VWA3B
  hgvsc: ENST00000448079.1:n.574T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.470T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*318T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12437T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.944T>C
  hgvsp: ENSP00000401959.1:p.Val315Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1150T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.944T>C
  hgvsp: ENSP00000411168.1:p.Val315Ala
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*631T>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val315Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

2-98750365-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750365
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750365
    reference: chr 2
allele count: 2
allele frequency: 1.65604040738594e-5
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1157T>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.501T>G
  hgvsp: ENST00000451075.2:c.501T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.951T>G
  hgvsp: ENST00000435344.1:c.951T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.951T>G
  hgvsp: ENST00000433678.1:c.951T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*638T>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.951T>G
  hgvsp: ENST00000477737.1:c.951T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.477T>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.951T>G
  hgvsp: ENST00000416277.1:c.951T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*325T>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12444T>G
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr317Thr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

2-98750368-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750368
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750368
    reference: chr 2
allele count: 3
allele frequency: 2.484142887898912e-5
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.954G>A
  hgvsp: ENSP00000388158.1:p.Trp318Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.954G>A
  hgvsp: ENSP00000401959.1:p.Trp318Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.954G>A
  hgvsp: ENSP00000417955.1:p.Trp318Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1160G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.954G>A
  hgvsp: ENSP00000411168.1:p.Trp318Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*328G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.504G>A
  hgvsp: ENSP00000389463.2:p.Trp168Ter
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*641G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12447G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.480G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Trp318Ter
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

2-98750371-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750371
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750371
    reference: chr 2
allele count: 3
allele frequency: 2.484184028352821e-5
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.483T>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*644T>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.957T>G
  hgvsp: ENSP00000411168.1:p.Asn319Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12450T>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.957T>G
  hgvsp: ENSP00000401959.1:p.Asn319Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.507T>G
  hgvsp: ENSP00000389463.2:p.Asn169Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.957T>G
  hgvsp: ENSP00000417955.1:p.Asn319Lys
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1163T>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*331T>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.957T>G
  hgvsp: ENSP00000388158.1:p.Asn319Lys
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5376
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn319Lys
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

2-98750377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750377
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750377
    reference: chr 2
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1169G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*650G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.489G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.963G>A
  hgvsp: ENST00000416277.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.963G>A
  hgvsp: ENST00000435344.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.963G>A
  hgvsp: ENST00000477737.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.513G>A
  hgvsp: ENST00000451075.2:c.513G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12456G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.963G>A
  hgvsp: ENST00000433678.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*337G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg321Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

2-98750388-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750388
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750387
    reference: chr 2
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*352delA
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.978delA
  hgvsp: ENSP00000401959.1:p.Lys326AsnfsTer74
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.978delA
  hgvsp: ENSP00000388158.1:p.Lys326AsnfsTer74
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1184delA
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.978delA
  hgvsp: ENSP00000411168.1:p.Lys326AsnfsTer58
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*665delA
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.978delA
  hgvsp: ENSP00000417955.1:p.Lys326AsnfsTer74
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12471delA
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.528delA
  hgvsp: ENSP00000389463.2:p.Lys176AsnfsTer74
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.504delA
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys326AsnfsTer74
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: GA
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

2-98750398-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750398
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750398
    reference: chr 2
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*671T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.984T>C
  hgvsp: ENST00000435344.1:c.984T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.534T>C
  hgvsp: ENST00000451075.2:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.984T>C
  hgvsp: ENST00000416277.1:c.984T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.984T>C
  hgvsp: ENST00000477737.1:c.984T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*358T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12477T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1190T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.984T>C
  hgvsp: ENST00000433678.1:c.984T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.510T>C
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8535
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro328Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

2-98750399-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750399
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750399
    reference: chr 2
allele count: 1
allele frequency: 8.284866862189524e-6
allele num: 120702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12478C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.985C>T
  hgvsp: ENSP00000417955.1:p.Pro329Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.985C>T
  hgvsp: ENSP00000401959.1:p.Pro329Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*359C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.985C>T
  hgvsp: ENSP00000411168.1:p.Pro329Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*672C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.535C>T
  hgvsp: ENSP00000389463.2:p.Pro179Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1191C>T
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.985C>T
  hgvsp: ENSP00000388158.1:p.Pro329Ser
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.511C>T
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro329Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

2-98750401-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750401
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750400
    reference: chr 2
allele count: 2
allele frequency: 1.657247974014352e-5
allele num: 120682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*362+1delG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1194+1delG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12482delG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.538+1delG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.988+1delG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*675+1delG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.988+1delG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.515delG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.988+1delG
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.988+1delG
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: AG
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

2-98750402-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750402
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750402
    reference: chr 2
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.988G>C
  hgvsp: ENSP00000401959.1:p.Gly330Arg
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1194G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*362G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.988G>C
  hgvsp: ENSP00000417955.1:p.Gly330Arg
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12481G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.514G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.988G>C
  hgvsp: ENSP00000411168.1:p.Gly330Arg
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*675G>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.538G>C
  hgvsp: ENSP00000389463.2:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.988G>C
  hgvsp: ENSP00000388158.1:p.Gly330Arg
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7288
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly330Arg
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

2-98750405-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750405
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750405
    reference: chr 2
allele count: 3
allele frequency: 2.486325211337643e-5
allele num: 120660
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.988+3A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.538+3A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.988+3A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.988+3A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*675+3A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1194+3A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*362+3A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.517A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.988+3A>G
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12484A>G
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7364
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.988+3A>G
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

2-98750408-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750408
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750408
    reference: chr 2
allele count: 1
allele frequency: 8.289674381590291e-6
allele num: 120632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.988+6T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.988+6T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.538+6T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12487T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*362+6T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1194+6T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.988+6T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.988+6T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*675+6T>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.520T>A
  variant of: http://identifiers.org/hgnc/28385
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.988+6T>A
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

2-98750421-A-AACATCATTCACAATTCTCTGTGCTATTCTGCCTCCCTGTCTTTTGCTTGTGGAATTGACAAGGTGCAGGAAGAAGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750421
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750497
    reference: chr 2
allele count: 1
allele frequency: 8.30137304710199e-6
allele num: 120462
alternate allele: AACATCATTCACAATTCTCTGTGCTATTCTGCCTCCCTGTCTTTTGCTTGTGGAATTGACAAGGTGCAGGAAGAAGC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7050
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4021
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

2-98750424-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750424
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750424
    reference: chr 2
allele count: 1
allele frequency: 8.304406317992327e-6
allele num: 120418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.536T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1194+22T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.988+22T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.988+22T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.538+22T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*675+22T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12503T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.988+22T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.988+22T>C
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*362+22T>C
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

2-98750428-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 98750428
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 98750428
    reference: chr 2
allele count: 1
allele frequency: 8.306889734345666e-6
allele num: 120382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000388158
  ensembl transcript: ENST00000433678
  gene symbol: VWA3B
  hgvsc: ENST00000433678.1:c.988+26G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000411168
  ensembl transcript: ENST00000416277
  gene symbol: VWA3B
  hgvsc: ENST00000416277.1:c.988+26G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000417955
  ensembl transcript: ENST00000477737
  gene symbol: VWA3B
  hgvsc: ENST00000477737.1:c.988+26G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000465930
  gene symbol: VWA3B
  hgvsc: ENST00000465930.1:n.540G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl transcript: ENST00000409460
  gene symbol: VWA3B
  hgvsc: ENST00000409460.1:n.1194+26G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396734
  ensembl transcript: ENST00000432242
  gene symbol: VWA3B
  hgvsc: ENST00000432242.1:c.*675+26G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000401959
  ensembl transcript: ENST00000435344
  gene symbol: VWA3B
  hgvsc: ENST00000435344.1:c.988+26G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000391241
  ensembl transcript: ENST00000422503
  gene symbol: VWA3B
  hgvsc: ENST00000422503.2:c.*362+26G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000389463
  ensembl transcript: ENST00000451075
  gene symbol: VWA3B
  hgvsc: ENST00000451075.2:c.538+26G>A
  variant of: http://identifiers.org/hgnc/28385
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168658
  ensembl protein: ENSP00000396866
  ensembl transcript: ENST00000448638
  gene symbol: VWA3B
  hgvsc: ENST00000448638.1:c.702+12507G>A
  variant of: http://identifiers.org/hgnc/28385
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2944
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32197
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7130
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3661
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1332
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

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: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

MQRankSum
type: SiteQuality
SIO_000300: 9.75e-1

QD
type: SiteQuality
SIO_000300: 1.412e1

DP
type: SiteQuality
SIO_000300: 2.047317e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.071e0

FS
type: SiteQuality
SIO_000300: 1.863e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.41e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-2

GenotypeDepth
all individuals: 7799
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2944
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1002
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9687
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3662
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7135
bin: 9.75e1
variant carriers: 84

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

GenotypeQuality
all individuals: 10
bin: 2.25e1
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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
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: 81
allele frequency: 8.263619669455213e-3
allele num: 9802
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

QD
type: SiteQuality
SIO_000300: 1.31e1

DP
type: SiteQuality
SIO_000300: 2.047743e6

VQSLOD
type: SiteQuality
SIO_000300: 4.69e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.388e0

GenotypeDepth
all individuals: 485
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3666
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2949
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 32255
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9697
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7074
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1002
bin: 8.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
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
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.955715279387897e-4
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.352e0

FS
type: SiteQuality
SIO_000300: 2.792e0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 2.037042e6

QD
type: SiteQuality
SIO_000300: 1.243e1

GenotypeDepth
all individuals: 15450
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9696
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1002
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2950
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32259
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3664
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7062
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 2399
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 2
allele frequency: 2.040399918384003e-4
allele num: 9802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

Other
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DP
type: SiteQuality
SIO_000300: 2.036347e6

ClippingRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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SIO_000300: 2.39e0

QD
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MQRankSum
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SIO_000300: 1.02e0

MQ
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SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

East Asian
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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QD
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DP
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SIO_000300: 2.035843e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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MQRankSum
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VQSLOD
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DP
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MQ
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BaseQRankSum
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SIO_000300: -1.147e0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.035544e6

ClippingRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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FS
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ReadPosRankSum
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QD
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InbreedingCoeff
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SIO_000300: 2.5e-3

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

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

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

Other
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African
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

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

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

European (Finnish)
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allele count: 1
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allele num: 6614
num of homozygotes: 0

South Asian
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Other
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African
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allele frequency: 2.041232904674423e-4
allele num: 9798
num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66736
num of homozygotes: 0

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

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

European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66714
num of homozygotes: 0

East Asian
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South Asian
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African
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Latino
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Other
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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FS
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16510
num of homozygotes: 0

African
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Other
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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ClippingRankSum
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ReadPosRankSum
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QD
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VQSLOD
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FS
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MQ
type: SiteQuality
SIO_000300: 5.921e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.99e0

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

DP
type: SiteQuality
SIO_000300: 2.032009e6

GenotypeDepth
all individuals: 1036
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2939
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32183
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7036
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9666
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3647
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
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: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 1.988e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

DP
type: SiteQuality
SIO_000300: 2.031912e6

QD
type: SiteQuality
SIO_000300: 1.19e1

GenotypeDepth
all individuals: 15402
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3647
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32181
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7034
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1332
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9667
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2940
bin: 7.25e1
variant carriers: 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: 1.499385252046661e-5
allele num: 66694
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: 9792
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.336e0

DP
type: SiteQuality
SIO_000300: 2.031647e6

VQSLOD
type: SiteQuality
SIO_000300: 1.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

QD
type: SiteQuality
SIO_000300: 1.274e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-2

FS
type: SiteQuality
SIO_000300: 8.72e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeDepth
all individuals: 797
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7033
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2939
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3647
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9662
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32120
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 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

African
type: Population
allele count: 1
allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.644e0

FS
type: SiteQuality
SIO_000300: 3.686e0

VQSLOD
type: SiteQuality
SIO_000300: -3.663e-1

DP
type: SiteQuality
SIO_000300: 2.031066e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.616e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

QD
type: SiteQuality
SIO_000300: 1.283e1

GenotypeDepth
all individuals: 483
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32123
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3645
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7032
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2939
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9662
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
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

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

African
type: Population
allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
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: -2.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.758e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.099e1

FS
type: SiteQuality
SIO_000300: 1.4514e1

QD
type: SiteQuality
SIO_000300: 7.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.042e-1

DP
type: SiteQuality
SIO_000300: 2.030613e6

GenotypeDepth
all individuals: 354
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 7025
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1326
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9637
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 175
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32037
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2932
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.022285831118381e-4
allele num: 9782
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: 0
allele frequency: 0.0e0
allele num: 66638
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: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 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: 16496
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

FS
type: SiteQuality
SIO_000300: 2.1854e1

MQRankSum
type: SiteQuality
SIO_000300: -5.26e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 2.028009e6

VQSLOD
type: SiteQuality
SIO_000300: -2.067e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.392e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

QD
type: SiteQuality
SIO_000300: 2.011e1

GenotypeDepth
all individuals: 7516
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 794
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3577
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 173
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7008
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 9547
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2885
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 121
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31541
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.100536847242558e-5
allele num: 16392
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: 0
allele frequency: 0.0e0
allele num: 11556
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: 9774
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.019889e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.703e0

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

QD
type: SiteQuality
SIO_000300: 1.023e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeDepth
all individuals: 231
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2883
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variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3566
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variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.75e1
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GenotypeQuality
all individuals: 9538
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31615
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2348
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7009
bin: 9.75e1
variant carriers: 4

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
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: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.44081034903588e-4
allele num: 16388
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e0

QD
type: SiteQuality
SIO_000300: 1.119e1

DP
type: SiteQuality
SIO_000300: 2.019696e6

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

GenotypeDepth
all individuals: 5383
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2654
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3559
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31528
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 7004
bin: 9.75e1
variant carriers: 1

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: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.884e1

DP
type: SiteQuality
SIO_000300: 2.017552e6

QD
type: SiteQuality
SIO_000300: 6.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.698e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.962e0

GenotypeQuality
all individuals: 31222
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.131207847946045e-5
allele num: 16310
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

DP
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.874e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

FS
type: SiteQuality
SIO_000300: 1.9391e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.98e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504755025881786e-5
allele num: 66456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.65e0

BaseQRankSum
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SIO_000300: -5.049e0

FS
type: SiteQuality
SIO_000300: 1.003e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.769e0

DP
type: SiteQuality
SIO_000300: 1.999947e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6989
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16164
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

MQ
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SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.990197e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

QD
type: SiteQuality
SIO_000300: 9.49e0

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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16134
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.013863773357444e-5
allele num: 66360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.452e0

DP
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SIO_000300: 1.981575e6

MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 7.1e-3

ClippingRankSum
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SIO_000300: -6.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

QD
type: SiteQuality
SIO_000300: 1.521e1

BaseQRankSum
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SIO_000300: 2.63e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.812524544603208e-4
allele num: 66206
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: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
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FS
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MQRankSum
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InbreedingCoeff
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SIO_000300: 4.2e-3

BaseQRankSum
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QD
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ClippingRankSum
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SIO_000300: -2.37e-1

ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.024986387561256e-5
allele num: 66116
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.267587780453797e-4
allele num: 15778
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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QD
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MQRankSum
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VQSLOD
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DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3171
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.895854398382204e-4
allele num: 15824
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.024803387779794e-5
allele num: 66120
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 6.886e0

BaseQRankSum
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SIO_000300: -2.419e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

InbreedingCoeff
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SIO_000300: 1.37e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

DP
type: SiteQuality
SIO_000300: 1.860323e6

QD
type: SiteQuality
SIO_000300: 1.307e1

GenotypeQuality
all individuals: 1012
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66120
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15824
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.332089552238806e-4
allele num: 8576
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.37e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

FS
type: SiteQuality
SIO_000300: 6.886e0

DP
type: SiteQuality
SIO_000300: 1.860323e6

QD
type: SiteQuality
SIO_000300: 1.307e1

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.419e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.409434687860531e-5
allele num: 15602
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.722e0

MQRankSum
type: SiteQuality
SIO_000300: 5.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

DP
type: SiteQuality
SIO_000300: 1.808445e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.69e-1

QD
type: SiteQuality
SIO_000300: 1.066e1

GenotypeQuality
all individuals: 2135
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7766
bin: 9.75e1
variant carriers: 1077

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 866
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2019
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variant carriers: 2

GenotypeQuality
all individuals: 2218
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variant carriers: 0

GenotypeQuality
all individuals: 15462
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2911
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 41
allele frequency: 3.583916083916084e-3
allele num: 11440
num of homozygotes: 0

South Asian
type: Population
allele count: 104
allele frequency: 6.657278197413904e-3
allele num: 15622
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.772009029345372e-3
allele num: 886
num of homozygotes: 0

African
type: Population
allele count: 22
allele frequency: 2.267106347897774e-3
allele num: 9704
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 61
allele frequency: 9.262071059823868e-3
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 856
allele frequency: 1.298504292952277e-2
allele num: 65922
num of homozygotes: 5

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 1.799352e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

QD
type: SiteQuality
SIO_000300: 1.506e1

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

GenotypeQuality
all individuals: 13305
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
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variant carriers: 0

GenotypeQuality
all individuals: 3516
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3433
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 217
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GenotypeQuality
all individuals: 2212
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GenotypeQuality
all individuals: 272
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 162
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variant carriers: 0

GenotypeQuality
all individuals: 6630
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variant carriers: 0

GenotypeQuality
all individuals: 1216
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variant carriers: 0

GenotypeQuality
all individuals: 6837
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variant carriers: 1

GenotypeQuality
all individuals: 2380
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variant carriers: 0

GenotypeQuality
all individuals: 5153
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.433350488934638e-5
allele num: 15544
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.554e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

DP
type: SiteQuality
SIO_000300: 1.782432e6

QD
type: SiteQuality
SIO_000300: 1.605e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5919
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GenotypeQuality
all individuals: 4349
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9628
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: 8448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15238
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528584530724549e-5
allele num: 65420
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
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QD
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SIO_000300: 1.198e1

ClippingRankSum
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SIO_000300: -1.275e0

ReadPosRankSum
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SIO_000300: 1.45e0

BaseQRankSum
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SIO_000300: 3.42e0

DP
type: SiteQuality
SIO_000300: 1.758119e6

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

VQSLOD
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SIO_000300: -2.012e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 2085
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16140
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: 2
allele frequency: 2.035830618892508e-4
allele num: 9824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66538
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

ClippingRankSum
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VQSLOD
type: SiteQuality
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FS
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BaseQRankSum
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SIO_000300: 7.8e-1

MQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.789999999999999e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4935
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GenotypeQuality
all individuals: 3608
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.019160211985324e-4
allele num: 9812
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: 896
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16016
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
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QD
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MQ
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
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SIO_000300: 1.257e0

DP
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.194e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66546
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 5.762795885487669e-3
allele num: 16138
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9820
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 1.160362032954282e-4
allele num: 8618
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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SIO_000300: 1.08e0

MQRankSum
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 2.860478e6

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16230
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
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MQ
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MQRankSum
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DP
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FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66576
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

European (Finnish)
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allele num: 6614
num of homozygotes: 0

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

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

East Asian
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num of homozygotes: 0

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

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

African
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Latino
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.999520038396928e-5
allele num: 66672
num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 3.023888720895071e-4
allele num: 6614
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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MQRankSum
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SIO_000300: 3.82e-1

FS
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ReadPosRankSum
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MQ
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 17

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12857
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2098
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25976
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 4070
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 28
allele frequency: 1.695941853422168e-3
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9820
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: 0
allele frequency: 0.0e0
allele num: 66702
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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.880998e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.154e0

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 5.56e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.66e-1

GenotypeDepth
all individuals: 1544
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5352
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 104
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variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12901
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2097
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3623
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25957
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
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: 9818
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: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 5.183e0

QD
type: SiteQuality
SIO_000300: 1.077e1

VQSLOD
type: SiteQuality
SIO_000300: -7.480000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.331e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 2.87864e6

GenotypeDepth
all individuals: 802
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4064
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variant carriers: 0

GenotypeQuality
all individuals: 12863
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4037
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26031
bin: 9.75e1
variant carriers: 174

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 5339
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 8.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 173
allele frequency: 1.047722868217054e-2
allele num: 16512
num of homozygotes: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9816
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
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: 2
allele frequency: 2.222222222222222e-3
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.361e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

FS
type: SiteQuality
SIO_000300: 5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.92e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 2.892118e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.81e-1

GenotypeDepth
all individuals: 4757
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4037
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2094
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12863
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26031
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4064
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5339
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 9816
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
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: 66722
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.92e-2

FS
type: SiteQuality
SIO_000300: 5.31e-1

DP
type: SiteQuality
SIO_000300: 2.892118e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

QD
type: SiteQuality
SIO_000300: 1.361e1

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.81e-1

GenotypeDepth
all individuals: 2298
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 25886
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5373
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4057
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4074
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12930
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3635
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
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: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
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: -7.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQ
type: SiteQuality
SIO_000300: 5.955e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.982e0

MQRankSum
type: SiteQuality
SIO_000300: -4.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.873991e6

QD
type: SiteQuality
SIO_000300: 1.134e1

VQSLOD
type: SiteQuality
SIO_000300: 9.18e-1

GenotypeDepth
all individuals: 4360
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2101
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 5374
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

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

GenotypeQuality
all individuals: 25883
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 4057
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3634
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12932
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4073
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
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: 66732
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: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 2.873541e6

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.84e-1

MQ
type: SiteQuality
SIO_000300: 6.044e1

QD
type: SiteQuality
SIO_000300: 1.694e1

FS
type: SiteQuality
SIO_000300: 2.437e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

GenotypeDepth
all individuals: 8572
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2101
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 25883
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 5.75e1
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GenotypeQuality
all individuals: 4075
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variant carriers: 0

GenotypeQuality
all individuals: 2313
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

FS
type: SiteQuality
SIO_000300: 4.737e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e0

VQSLOD
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SIO_000300: -4.039e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.334e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
SIO_000300: 2.8735e6

QD
type: SiteQuality
SIO_000300: 5.09e0

GenotypeDepth
all individuals: 2298
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 12934
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 2312
bin: 7.25e1
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GenotypeQuality
all individuals: 3635
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -3.34e-1

BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.977e1

ReadPosRankSum
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SIO_000300: 9.82e-1

FS
type: SiteQuality
SIO_000300: 6.09e-1

QD
type: SiteQuality
SIO_000300: 1.098e1

DP
type: SiteQuality
SIO_000300: 2.873486e6

GenotypeDepth
all individuals: 8575
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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: 8.25e1
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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

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

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

East Asian
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DP
type: SiteQuality
SIO_000300: 2.873473e6

VQSLOD
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SIO_000300: 6.830000000000001e-1

InbreedingCoeff
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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QD
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SIO_000300: 1.459e1

ClippingRankSum
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SIO_000300: -1.6e-2

BaseQRankSum
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SIO_000300: 4.58e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9808
num of homozygotes: 0

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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VQSLOD
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FS
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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MQ
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

BaseQRankSum
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SIO_000300: 2.23e-1

MQ
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DP
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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QD
type: SiteQuality
SIO_000300: 1.256e1

ClippingRankSum
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SIO_000300: 1.82e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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Latino
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allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

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

African
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allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66738
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European (Finnish)
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
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allele num: 66738
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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African
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South Asian
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Latino
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MQ
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

Latino
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-1

DP
type: SiteQuality
SIO_000300: 2.871966e6

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.147e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 1.973e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.34e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
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)
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allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

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

VQSLOD
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SIO_000300: 1.48e0

FS
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BaseQRankSum
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MQRankSum
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SIO_000300: 4.58e-1

InbreedingCoeff
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SIO_000300: 8.0e-4

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

DP
type: SiteQuality
SIO_000300: 2.871788e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

African
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allele count: 3
allele frequency: 3.059975520195838e-4
allele num: 9804
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.786e0

BaseQRankSum
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SIO_000300: 1.59e0

VQSLOD
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SIO_000300: 1.21e0

ReadPosRankSum
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SIO_000300: 1.69e0

InbreedingCoeff
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SIO_000300: 1.0e-3

MQRankSum
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SIO_000300: 2.84e-1

ClippingRankSum
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SIO_000300: -1.515e0

MQ
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SIO_000300: 5.923e1

DP
type: SiteQuality
SIO_000300: 2.871501e6

QD
type: SiteQuality
SIO_000300: 1.487e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.211e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 7.0e-4

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.136e1

FS
type: SiteQuality
SIO_000300: 1.2439e1

DP
type: SiteQuality
SIO_000300: 2.871141e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

BaseQRankSum
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SIO_000300: 5.27e-1

MQ
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SIO_000300: 6.067e1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 7.833e0

MQRankSum
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VQSLOD
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QD
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SIO_000300: 1.28e1

DP
type: SiteQuality
SIO_000300: 2.870616e6

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
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allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 2.0e-4

MQRankSum
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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DP
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QD
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VQSLOD
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BaseQRankSum
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SIO_000300: 4.9e0

GenotypeQuality
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variant carriers: 0

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

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

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

Other
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.999220202747286e-5
allele num: 66684
num of homozygotes: 0

South Asian
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East Asian
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Other
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ReadPosRankSum
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InbreedingCoeff
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MQ
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DP
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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FS
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VQSLOD
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5338
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 8.75e1
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: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 7.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

FS
type: SiteQuality
SIO_000300: 5.441e0

DP
type: SiteQuality
SIO_000300: 2.867455e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.054e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.232e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.098e1

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

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

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4068
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 137
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12711
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
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: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500045000450004e-5
allele num: 66666
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.866669e6

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.55e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.38e-1

GenotypeQuality
all individuals: 12678
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4045
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25861
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5325
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3632
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4068
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2290
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
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: -2.78e-1

DP
type: SiteQuality
SIO_000300: 2.865485e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: -8.074e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 2.835e0

QD
type: SiteQuality
SIO_000300: 1.847e1

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

GenotypeQuality
all individuals: 477
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12210
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2097
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25853
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3625
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5245
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4057
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503352476021528e-5
allele num: 66518
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
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: 8598
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.52e-1

FS
type: SiteQuality
SIO_000300: 3.4365e1

DP
type: SiteQuality
SIO_000300: 2.85685e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.122e1

MQ
type: SiteQuality
SIO_000300: 5.648e1

VQSLOD
type: SiteQuality
SIO_000300: -6.772e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.18e-1

QD
type: SiteQuality
SIO_000300: 1.0e-1

GenotypeQuality
all individuals: 186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25851
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3625
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2275
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4010
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5195
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11918
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.53e-1

QD
type: SiteQuality
SIO_000300: 1.542e1

DP
type: SiteQuality
SIO_000300: 2.852896e6

VQSLOD
type: SiteQuality
SIO_000300: -5.22e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.661e0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3620
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variant carriers: 0

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

GenotypeQuality
all individuals: 215
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variant carriers: 0

GenotypeQuality
all individuals: 5089
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variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 25846
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11615
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3992
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 8.75e1
variant carriers: 0