15-65899548-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899548
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899548
    reference: chr 15
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.273A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*378A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.171A>G
  hgvsp: ENST00000395644.4:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+92A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+92A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.171A>G
  hgvsp: ENST00000569004.1:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*395A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.171A>G
  hgvsp: ENST00000442903.3:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.279A>G
  hgvsp: ENST00000567744.1:c.279A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-1974A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*505A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-1974A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-1974A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.171A>G
  hgvsp: ENST00000313182.2:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.267A>G
  hgvsp: ENST00000567923.1:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+92A>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15669
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser89Ser
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

15-65899549-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899549
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899550
    reference: chr 15
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.277dupT
  hgvsp: ENSP00000457624.1:p.Ser93PhefsTer15
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-1976dupT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+90dupT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.265dupT
  hgvsp: ENSP00000454425.1:p.Ser89PhefsTer15
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-1976dupT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*376dupT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-1976dupT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.169dupT
  hgvsp: ENSP00000379006.4:p.Ser57PhefsTer15
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.169dupT
  hgvsp: ENSP00000396314.3:p.Ser57PhefsTer15
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.169dupT
  hgvsp: ENSP00000326379.2:p.Ser57PhefsTer15
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*503dupT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.169dupT
  hgvsp: ENSP00000455105.1:p.Ser57PhefsTer15
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+90dupT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+90dupT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.271dupT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*393dupT
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser89PhefsTer15
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

15-65899562-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899562
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899562
    reference: chr 15
allele count: 13
allele frequency: 1.071405024065405e-4
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.157C>T
  hgvsp: ENSP00000455105.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+78C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+78C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+78C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-1988C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*364C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.265C>T
  hgvsp: ENSP00000457624.1:p.Leu89Phe
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*491C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*381C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.157C>T
  hgvsp: ENSP00000396314.3:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.253C>T
  hgvsp: ENSP00000454425.1:p.Leu85Phe
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.259C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.157C>T
  hgvsp: ENSP00000379006.4:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.157C>T
  hgvsp: ENSP00000326379.2:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-1988C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-1988C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Leu85Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/15-65899575-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899575
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899575
    reference: chr 15
allele count: 3
allele frequency: 2.472024918011174e-5
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.144T>G
  hgvsp: ENST00000442903.3:c.144T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.144T>G
  hgvsp: ENST00000313182.2:c.144T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*368T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.144T>G
  hgvsp: ENST00000395644.4:c.144T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.246T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*351T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+65T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2001T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+65T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2001T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.252T>G
  hgvsp: ENST00000567744.1:c.252T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.144T>G
  hgvsp: ENST00000569004.1:c.144T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*478T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+65T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2001T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.240T>G
  hgvsp: ENST00000567923.1:c.240T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu80Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

15-65899595-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899595
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899595
    reference: chr 15
allele count: 3
allele frequency: 2.471699045924168e-5
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.232A>G
  hgvsp: ENSP00000457624.1:p.Met78Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+45A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.124A>G
  hgvsp: ENSP00000326379.2:p.Met42Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2021A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2021A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.124A>G
  hgvsp: ENSP00000455105.1:p.Met42Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2021A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*331A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.124A>G
  hgvsp: ENSP00000379006.4:p.Met42Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.226A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*348A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*458A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.124A>G
  hgvsp: ENSP00000396314.3:p.Met42Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+45A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+45A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.220A>G
  hgvsp: ENSP00000454425.1:p.Met74Val
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Met74Val
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

15-65899600-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899600
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899600
    reference: chr 15
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.119A>C
  hgvsp: ENSP00000326379.2:p.Glu40Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+40A>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.119A>C
  hgvsp: ENSP00000379006.4:p.Glu40Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*326A>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2026A>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.119A>C
  hgvsp: ENSP00000396314.3:p.Glu40Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*453A>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2026A>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.119A>C
  hgvsp: ENSP00000455105.1:p.Glu40Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+40A>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.215A>C
  hgvsp: ENSP00000454425.1:p.Glu72Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*343A>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.227A>C
  hgvsp: ENSP00000457624.1:p.Glu76Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2026A>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.221A>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+40A>C
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16092
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu72Ala
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-65899611-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899611
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899611
    reference: chr 15
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+29G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*332G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2037G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.210G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*315G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.108G>T
  hgvsp: ENST00000313182.2:c.108G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.108G>T
  hgvsp: ENST00000569004.1:c.108G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.216G>T
  hgvsp: ENST00000567744.1:c.216G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.204G>T
  hgvsp: ENST00000567923.1:c.204G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.108G>T
  hgvsp: ENST00000442903.3:c.108G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.108G>T
  hgvsp: ENST00000395644.4:c.108G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+29G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2037G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2037G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+29G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*442G>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr68Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

15-65899611-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899611
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899611
    reference: chr 15
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.210G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.204G>A
  hgvsp: ENST00000567923.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*332G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2037G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.216G>A
  hgvsp: ENST00000567744.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2037G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+29G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.108G>A
  hgvsp: ENST00000569004.1:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.108G>A
  hgvsp: ENST00000395644.4:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*442G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.108G>A
  hgvsp: ENST00000313182.2:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+29G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.108G>A
  hgvsp: ENST00000442903.3:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2037G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*315G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+29G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39938
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr68Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

15-65899612-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899612
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899612
    reference: chr 15
allele count: 9
allele frequency: 7.41521932570939e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.203C>T
  hgvsp: ENSP00000454425.1:p.Thr68Met
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2038C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*331C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2038C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.107C>T
  hgvsp: ENSP00000326379.2:p.Thr36Met
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*314C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.107C>T
  hgvsp: ENSP00000379006.4:p.Thr36Met
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.209C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.107C>T
  hgvsp: ENSP00000396314.3:p.Thr36Met
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.107C>T
  hgvsp: ENSP00000455105.1:p.Thr36Met
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.215C>T
  hgvsp: ENSP00000457624.1:p.Thr72Met
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2038C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*441C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr68Met
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

15-65899625-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899625
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899625
    reference: chr 15
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.94G>A
  hgvsp: ENSP00000396314.3:p.Ala32Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*301G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*428G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.94G>A
  hgvsp: ENSP00000455105.1:p.Ala32Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2051G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.94G>A
  hgvsp: ENSP00000326379.2:p.Ala32Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.94G>A
  hgvsp: ENSP00000379006.4:p.Ala32Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.202G>A
  hgvsp: ENSP00000457624.1:p.Ala68Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+15G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2051G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.190G>A
  hgvsp: ENSP00000454425.1:p.Ala64Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*318G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2051G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.196G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+15G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+15G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala64Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

15-65899634-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899634
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899634
    reference: chr 15
allele count: 6
allele frequency: 4.943886883868097e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+6C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.181C>A
  hgvsp: ENSP00000454425.1:p.His61Asn
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.193C>A
  hgvsp: ENSP00000457624.1:p.His65Asn
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.85C>A
  hgvsp: ENSP00000326379.2:p.His29Asn
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*309C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*419C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.85C>A
  hgvsp: ENSP00000396314.3:p.His29Asn
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.187C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.85C>A
  hgvsp: ENSP00000379006.4:p.His29Asn
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2060C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+6C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2060C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*292C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.85C>A
  hgvsp: ENSP00000455105.1:p.His29Asn
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+6C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2060C>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His61Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-65899639-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899639
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899639
    reference: chr 15
allele count: 7
allele frequency: 5.768723628691983e-5
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2065G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*304G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.176G>A
  hgvsp: ENSP00000454425.1:p.Arg59His
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.188G>A
  hgvsp: ENSP00000457624.1:p.Arg63His
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.80G>A
  hgvsp: ENSP00000396314.3:p.Arg27His
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2065G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79+1G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*287G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.80G>A
  hgvsp: ENSP00000326379.2:p.Arg27His
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.80G>A
  hgvsp: ENSP00000379006.4:p.Arg27His
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79+1G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16+1G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.182G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2065G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.80G>A
  hgvsp: ENSP00000455105.1:p.Arg27His
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*414G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.79+1G>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

15-65899640-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899640
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899640
    reference: chr 15
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2066C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.79C>T
  hgvsp: ENSP00000326379.2:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.175C>T
  hgvsp: ENSP00000454425.1:p.Arg59Cys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*413C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*286C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.79C>T
  hgvsp: ENSP00000379006.4:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.79C>T
  hgvsp: ENSP00000456460.1:p.Pro27Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*303C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2066C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.79C>T
  hgvsp: ENSP00000455105.1:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.79C>T
  hgvsp: ENSP00000457922.1:p.Pro27Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2066C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.181C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.79C>T
  hgvsp: ENSP00000396314.3:p.Arg27Cys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-16C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.187C>T
  hgvsp: ENSP00000457624.1:p.Arg63Cys
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg27Cys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

15-65899647-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899647
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899647
    reference: chr 15
allele count: 2
allele frequency: 1.648451280022419e-5
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.180A>G
  hgvsp: ENST00000567744.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-23A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.174A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*406A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2073A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.72A>G
  hgvsp: ENST00000568573.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.72A>G
  hgvsp: ENST00000313182.2:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.168A>G
  hgvsp: ENST00000567923.1:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.72A>G
  hgvsp: ENST00000395644.4:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2073A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.72A>G
  hgvsp: ENST00000442903.3:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2073A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*279A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*296A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.72A>G
  hgvsp: ENST00000569491.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.72A>G
  hgvsp: ENST00000569004.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu24Glu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

15-65899652-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899652
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899652
    reference: chr 15
allele count: 3
allele frequency: 2.473166147301776e-5
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*274G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.67G>A
  hgvsp: ENSP00000379006.4:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.67G>A
  hgvsp: ENSP00000457922.1:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.67G>A
  hgvsp: ENSP00000456460.1:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.67G>A
  hgvsp: ENSP00000455105.1:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.67G>A
  hgvsp: ENSP00000396314.3:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2078G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-28G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.67G>A
  hgvsp: ENSP00000326379.2:p.Glu23Lys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.163G>A
  hgvsp: ENSP00000454425.1:p.Glu55Lys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.175G>A
  hgvsp: ENSP00000457624.1:p.Glu59Lys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2078G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2078G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.169G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*401G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*291G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu23Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

15-65899653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899653
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899653
    reference: chr 15
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.66C>T
  hgvsp: ENST00000442903.3:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.162C>T
  hgvsp: ENST00000567923.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-29C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.168C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.66C>T
  hgvsp: ENST00000569491.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*290C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2079C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*273C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.66C>T
  hgvsp: ENST00000568573.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*400C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.174C>T
  hgvsp: ENST00000567744.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.66C>T
  hgvsp: ENST00000313182.2:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.66C>T
  hgvsp: ENST00000569004.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.66C>T
  hgvsp: ENST00000395644.4:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2079C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2079C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser22Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD

15-65899657-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899657
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899657
    reference: chr 15
allele count: 3
allele frequency: 2.473370049137618e-5
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2083G>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-33G>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.62G>C
  hgvsp: ENSP00000456460.1:p.Gly21Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*286G>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.62G>C
  hgvsp: ENSP00000455105.1:p.Gly21Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.164G>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.62G>C
  hgvsp: ENSP00000379006.4:p.Gly21Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.158G>C
  hgvsp: ENSP00000454425.1:p.Gly53Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.62G>C
  hgvsp: ENSP00000396314.3:p.Gly21Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.62G>C
  hgvsp: ENSP00000326379.2:p.Gly21Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2083G>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.62G>C
  hgvsp: ENSP00000457922.1:p.Gly21Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2083G>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*269G>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.170G>C
  hgvsp: ENSP00000457624.1:p.Gly57Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*396G>C
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly21Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

15-65899657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899657
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899657
    reference: chr 15
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.62G>A
  hgvsp: ENSP00000457922.1:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*286G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*269G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*396G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.62G>A
  hgvsp: ENSP00000379006.4:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.158G>A
  hgvsp: ENSP00000454425.1:p.Gly53Glu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.170G>A
  hgvsp: ENSP00000457624.1:p.Gly57Glu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.62G>A
  hgvsp: ENSP00000396314.3:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-33G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2083G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2083G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.62G>A
  hgvsp: ENSP00000455105.1:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.62G>A
  hgvsp: ENSP00000456460.1:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.164G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2083G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.62G>A
  hgvsp: ENSP00000326379.2:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly21Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

15-65899659-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899659
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899659
    reference: chr 15
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.156G>A
  hgvsp: ENST00000567923.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.60G>A
  hgvsp: ENST00000568573.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*267G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.60G>A
  hgvsp: ENST00000569491.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.60G>A
  hgvsp: ENST00000442903.3:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.168G>A
  hgvsp: ENST00000567744.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*394G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*284G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2085G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2085G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.60G>A
  hgvsp: ENST00000569004.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.60G>A
  hgvsp: ENST00000313182.2:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.60G>A
  hgvsp: ENST00000395644.4:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2085G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-35G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.162G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu20Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

15-65899663-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899663
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899663
    reference: chr 15
allele count: 3
allele frequency: 2.474185992808366e-5
allele num: 121252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.56T>C
  hgvsp: ENSP00000379006.4:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2089T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*280T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.152T>C
  hgvsp: ENSP00000454425.1:p.Ile51Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.56T>C
  hgvsp: ENSP00000455105.1:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.56T>C
  hgvsp: ENSP00000326379.2:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.158T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.56T>C
  hgvsp: ENSP00000456460.1:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.56T>C
  hgvsp: ENSP00000457922.1:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-39T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.56T>C
  hgvsp: ENSP00000396314.3:p.Ile19Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2089T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*390T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2089T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.164T>C
  hgvsp: ENSP00000457624.1:p.Ile55Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*263T>C
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile19Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

15-65899664-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899664
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899664
    reference: chr 15
allele count: 6
allele frequency: 4.949351634935823e-5
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.55A>G
  hgvsp: ENSP00000456460.1:p.Ile19Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.163A>G
  hgvsp: ENSP00000457624.1:p.Ile55Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2090A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.55A>G
  hgvsp: ENSP00000326379.2:p.Ile19Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*389A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.151A>G
  hgvsp: ENSP00000454425.1:p.Ile51Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.55A>G
  hgvsp: ENSP00000455105.1:p.Ile19Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.55A>G
  hgvsp: ENSP00000396314.3:p.Ile19Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.157A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.55A>G
  hgvsp: ENSP00000379006.4:p.Ile19Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2090A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.55A>G
  hgvsp: ENSP00000457922.1:p.Ile19Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*279A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2090A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*262A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-40A>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile19Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

15-65899673-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899673
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899673
    reference: chr 15
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-49C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2099C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.46C>T
  hgvsp: ENSP00000456460.1:p.Pro16Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.142C>T
  hgvsp: ENSP00000454425.1:p.Pro48Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.46C>T
  hgvsp: ENSP00000379006.4:p.Pro16Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.148C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.46C>T
  hgvsp: ENSP00000396314.3:p.Pro16Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*380C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.46C>T
  hgvsp: ENSP00000455105.1:p.Pro16Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.154C>T
  hgvsp: ENSP00000457624.1:p.Pro52Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2099C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.46C>T
  hgvsp: ENSP00000457922.1:p.Pro16Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*270C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.46C>T
  hgvsp: ENSP00000326379.2:p.Pro16Ser
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2099C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*253C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro16Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/15-65899675-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899675
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899675
    reference: chr 15
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.140G>T
  hgvsp: ENSP00000454425.1:p.Arg47Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*268G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.152G>T
  hgvsp: ENSP00000457624.1:p.Arg51Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.146G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2101G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*378G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.44G>T
  hgvsp: ENSP00000457922.1:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.44G>T
  hgvsp: ENSP00000456460.1:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.44G>T
  hgvsp: ENSP00000326379.2:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.44G>T
  hgvsp: ENSP00000455105.1:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.44G>T
  hgvsp: ENSP00000396314.3:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-51G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2101G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2101G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*251G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.44G>T
  hgvsp: ENSP00000379006.4:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg15Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

15-65899698-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899698
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899698
    reference: chr 15
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-74G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*355G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.21G>A
  hgvsp: ENSP00000457922.1:p.Met7Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*245G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2124G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2124G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.21G>A
  hgvsp: ENSP00000455105.1:p.Met7Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.123G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*228G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.21G>A
  hgvsp: ENSP00000396314.3:p.Met7Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.21G>A
  hgvsp: ENSP00000456460.1:p.Met7Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.117G>A
  hgvsp: ENSP00000454425.1:p.Met39Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.129G>A
  hgvsp: ENSP00000457624.1:p.Met43Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.21G>A
  hgvsp: ENSP00000379006.4:p.Met7Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2124G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.21G>A
  hgvsp: ENSP00000326379.2:p.Met7Ile
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38722
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met7Ile
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-65899703-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899703
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899703
    reference: chr 15
allele count: 2
allele frequency: 1.668919708272835e-5
allele num: 119838
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*240G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.16G>A
  hgvsp: ENSP00000455105.1:p.Val6Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.16G>A
  hgvsp: ENSP00000326379.2:p.Val6Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.16G>A
  hgvsp: ENSP00000396314.3:p.Val6Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.16G>A
  hgvsp: ENSP00000457922.1:p.Val6Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.16G>A
  hgvsp: ENSP00000379006.4:p.Val6Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.16G>A
  hgvsp: ENSP00000456460.1:p.Val6Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.112G>A
  hgvsp: ENSP00000454425.1:p.Val38Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.124G>A
  hgvsp: ENSP00000457624.1:p.Val42Ile
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-79G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*350G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*223G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.118G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2129G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2129G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2129G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16264
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val6Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

15-65899713-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899713
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899713
    reference: chr 15
allele count: 1
allele frequency: 8.430423713095819e-6
allele num: 118618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.6G>A
  hgvsp: ENST00000569491.1:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-89G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2139G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.6G>A
  hgvsp: ENST00000313182.2:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2139G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.6G>A
  hgvsp: ENST00000442903.3:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.108G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.6G>A
  hgvsp: ENST00000568573.1:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.102G>A
  hgvsp: ENST00000567923.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.6G>A
  hgvsp: ENST00000395644.4:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*213G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*230G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*340G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2139G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.6G>A
  hgvsp: ENST00000569004.1:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.114G>A
  hgvsp: ENST00000567744.1:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro2Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/15-65899742-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899742
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899742
    reference: chr 15
allele count: 3
allele frequency: 2.805416323782449e-5
allele num: 106936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2168G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*201G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-24G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-118G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-24G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-24G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-24G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.79G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.85G>T
  hgvsp: ENSP00000457624.1:p.Gly29Trp
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.73G>T
  hgvsp: ENSP00000454425.1:p.Gly25Trp
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2168G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2168G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.-24G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-24G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*184G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*311G>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27895
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly25Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/15-65899747-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899747
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899747
    reference: chr 15
allele count: 1
allele frequency: 9.630756784868155e-6
allele num: 103834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-29T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2173T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*306T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-29T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-29T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.68T>G
  hgvsp: ENSP00000454425.1:p.Leu23Arg
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*179T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.80T>G
  hgvsp: ENSP00000457624.1:p.Leu27Arg
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-29T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-123T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-29T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.-29T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.74T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*196T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2173T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2173T>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu23Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

15-65899747-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899747
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899747
    reference: chr 15
allele count: 1
allele frequency: 9.630756784868155e-6
allele num: 103834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.74T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-123T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-29T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*179T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.80T>C
  hgvsp: ENSP00000457624.1:p.Leu27Pro
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-29T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2173T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-29T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-29T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2173T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000455105
  ensembl transcript: ENST00000569004
  gene symbol: VWA9
  hgvsc: ENST00000569004.1:c.-29T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2173T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.68T>C
  hgvsp: ENSP00000454425.1:p.Leu23Pro
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*196T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*306T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-29T>C
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu23Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-65899749-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899749
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899749
    reference: chr 15
allele count: 1
allele frequency: 9.794127441186264e-6
allele num: 102102
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2175T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-31T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.72T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2175T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-31T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-125T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-31T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-31T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2175T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-31T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.66T>G
  hgvsp: ENSP00000454425.1:p.Ile22Met
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.78T>G
  hgvsp: ENSP00000457624.1:p.Ile26Met
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*304T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*194T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*177T>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile22Met
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

15-65899751-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899751
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899751
    reference: chr 15
allele count: 1
allele frequency: 9.936999423654034e-6
allele num: 100634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.64A>G
  hgvsp: ENSP00000454425.1:p.Ile22Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-33A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*192A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.76A>G
  hgvsp: ENSP00000457624.1:p.Ile26Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-33A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-33A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-127A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-33A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2177A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2177A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*302A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*175A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2177A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.70A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-33A>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11359
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile22Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/15-65899754-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899754
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899754
    reference: chr 15
allele count: 1
allele frequency: 1.022097753429138e-5
allele num: 97838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.73T>G
  hgvsp: ENSP00000457624.1:p.Cys25Gly
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-36T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-36T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.61T>G
  hgvsp: ENSP00000454425.1:p.Cys21Gly
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-36T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.67T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-36T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*172T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-130T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-36T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*299T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2180T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*189T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2180T>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2180T>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20455
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12367
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys21Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

15-65899755-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899755
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899755
    reference: chr 15
allele count: 4
allele frequency: 4.121077249593044e-5
allele num: 97062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*298T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*188T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*171T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-37T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-37T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-131T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-37T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.60T>C
  hgvsp: ENST00000567923.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-37T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.72T>C
  hgvsp: ENST00000567744.1:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2181T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2181T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.66T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2181T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-37T>C
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19791
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val20Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

15-65899771-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899771
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899771
    reference: chr 15
allele count: 2
allele frequency: 2.445346505599844e-5
allele num: 81788
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2197G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2197G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*172G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2197G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-45-8G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-53G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-53G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*282G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.64-8G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-147G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*163-8G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.58-8G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-53G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-53G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.52-8G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.64-8G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

15-65899772-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899772
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899772
    reference: chr 15
allele count: 1
allele frequency: 1.227656648988411e-5
allele num: 81456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-54C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-54C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-54C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.64-9C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-54C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2198C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*281C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-45-9C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2198C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.58-9C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-148C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2198C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*171C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.52-9C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*163-9C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

15-65899780-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899780
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899780
    reference: chr 15
allele count: 1
allele frequency: 1.351935972312351e-5
allele num: 73968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-62C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-45-17C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2206C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.58-17C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2206C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-156C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*163C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*273C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2206C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-62C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.52-17C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-62C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-62C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*163-17C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.64-17C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*273C>T
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

15-65899795-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899795
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899795
    reference: chr 15
allele count: 2
allele frequency: 3.251926766609216e-5
allele num: 61502
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.64-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-62-15A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2221A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*273-15A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.58-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2221A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.52-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-62-15A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-62-15A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2221A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-45-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-62-15A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*163-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-156-15A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*163-15A>G
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-65899797-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899797
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899797
    reference: chr 15
allele count: 1
allele frequency: 1.660191918185742e-5
allele num: 60234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-62-17G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.64-34G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*163-17G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-45-34G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.52-34G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-156-17G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.58-34G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2223G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-62-17G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-62-17G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2223G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*163-34G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2223G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-62-17G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*273-17G>T
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18792
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19981
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

15-65899797-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899797
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899797
    reference: chr 15
allele count: 1
allele frequency: 1.660191918185742e-5
allele num: 60234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-45-34G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.58-34G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-62-17G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-62-17G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2223G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*163-17G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2223G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.64-34G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*273-17G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-62-17G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2223G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*163-34G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-156-17G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.52-34G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-62-17G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19981
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

15-65899806-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899806
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899806
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 49950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-62-26T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2232T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-62-26T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-156-26T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-62-26T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-62-26T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-45-43T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*163-43T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.64-43T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*273-26T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2232T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2232T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.52-43T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.58-43T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*163-26T>C
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10460
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23937
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14176
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

15-65899808-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899808
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899808
    reference: chr 15
allele count: 1
allele frequency: 2.206433961431534e-5
allele num: 45322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.52-45C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2234C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-62-28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2234C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-62-28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-156-28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.64-45C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-62-28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*163-28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*163-45C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-62-28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*273-28C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2234C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.58-45C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-45-45C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12801
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10588
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS

15-65899812-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65899812
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65899812
    reference: chr 15
allele count: 1
allele frequency: 2.37676474782526e-5
allele num: 42074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-15-2238A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.58-49A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-62-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.52-2238A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-156-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-62-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.64-49A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-62-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*163-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-62-32A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.52-49A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-45-49A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.64-2238A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*163-49A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*273-32A>G
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12228
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25660
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

15-65903005-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903005
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903005
    reference: chr 15
allele count: 2
allele frequency: 1.857355126300148e-4
allele num: 10768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.63+19A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+431A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+431A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+431A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+431A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+431A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-63+129A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-16+129A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-63+129A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*162+129A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+431A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+431A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*272+19A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*162+129A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.63+19A>G
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS

15-65903013-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903013
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903013
    reference: chr 15
allele count: 2
allele frequency: 1.857010213556174e-4
allele num: 10770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*162+121A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*162+121A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.63+11A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+423A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.63+11A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-63+121A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+423A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-16+121A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+423A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+423A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+423A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+423A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*272+11A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-63+121A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+423A>G
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

15-65903017-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903017
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903017
    reference: chr 15
allele count: 1
allele frequency: 9.288500835965076e-5
allele num: 10766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*272+7C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-63+117C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+419C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+419C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+419C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+419C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*162+117C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.63+7C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+419C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.63+7C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-16+117C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*162+117C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+419C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+419C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-63+117C>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*272+7C>A
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

15-65903121-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903121
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903121
    reference: chr 15
allele count: 1
allele frequency: 9.29022668153103e-5
allele num: 10764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+315C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*162+13C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+315C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+315C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+315C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-16+13C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+315C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-63+13C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*175C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+315C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+315C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-63+13C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*162+13C>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

15-65903122-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903122
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903122
    reference: chr 15
allele count: 1
allele frequency: 9.288500835965076e-5
allele num: 10766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+314T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-36T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+314T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*174T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+314T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-36T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-63+12T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+314T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+314T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+314T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-16+12T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*162+12T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*162+12T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-63+12T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+314T>C
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

15-65903286-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903286
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903286
    reference: chr 15
allele count: 12
allele frequency: 6.0790273556231e-3
allele num: 1974
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+150T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+150T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*10T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-200T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-215T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*10T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-168T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+150T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-215T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-200T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*10T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+150T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+150T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+150T>C
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+150T>C
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/15-65903292-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903292
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903292
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 2090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+144G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-221G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+144G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.*4G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.*4G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+144G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+144G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-174G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+144G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-221G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+144G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-206G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-206G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.*4G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+144G>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

15-65903297-CACAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903297
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903293
    reference: chr 15
allele count: 2
allele frequency: 8.710801393728223e-4
allele num: 2296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+135_57+138delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-230_-227delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-183_-180delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+135_-63+138delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+135_51+138delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-230_-227delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+135_-157+138delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-215_-212delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.169_172delCTGT
  hgvsp: ENSP00000454972.1:p.Leu57Glu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.169_172delCTGT
  hgvsp: ENSP00000457977.1:p.Leu57Glu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-215_-212delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+135_51+138delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+135_-63+138delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+135_-46+138delCTGT
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.169_172delCTGT
  hgvsp: ENSP00000458470.1:p.Leu57Glu
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu57Glu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: CACAG
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

15-65903326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903326
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903326
    reference: chr 15
allele count: 1
allele frequency: 2.288329519450801e-4
allele num: 4370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+110C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-240C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-240C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+110C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-208C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-255C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-255C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.144C>T
  hgvsp: ENST00000567940.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+110C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+110C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.144C>T
  hgvsp: ENST00000569565.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+110C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.144C>T
  hgvsp: ENST00000573314.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+110C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+110C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala48Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

15-65903340-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903340
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903340
    reference: chr 15
allele count: 1
allele frequency: 1.613423685059697e-4
allele num: 6198
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+96C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.130C>G
  hgvsp: ENSP00000457977.1:p.Leu44Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.130C>G
  hgvsp: ENSP00000458470.1:p.Leu44Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+96C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-222C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+96C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-254C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-269C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.130C>G
  hgvsp: ENSP00000454972.1:p.Leu44Val
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-254C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-269C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+96C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+96C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+96C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+96C>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu44Val
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

15-65903345-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903345
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903345
    reference: chr 15
allele count: 1
allele frequency: 1.385041551246538e-4
allele num: 7220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+91C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.125C>G
  hgvsp: ENSP00000454972.1:p.Pro42Arg
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+91C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+91C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.125C>G
  hgvsp: ENSP00000458470.1:p.Pro42Arg
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-227C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+91C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-274C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.125C>G
  hgvsp: ENSP00000457977.1:p.Pro42Arg
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-259C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+91C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+91C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-259C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+91C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-274C>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro42Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

15-65903347-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903347
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903347
    reference: chr 15
allele count: 3
allele frequency: 3.989361702127659e-4
allele num: 7520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.123G>A
  hgvsp: ENST00000569565.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.123G>A
  hgvsp: ENST00000573314.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.123G>A
  hgvsp: ENST00000567940.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+89G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+89G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-276G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+89G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-276G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-229G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-261G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+89G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+89G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+89G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+89G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-261G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly41Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

15-65903359-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903359
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903359
    reference: chr 15
allele count: 8
allele frequency: 8.178286648947046e-4
allele num: 9782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-241G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-288G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-273G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.111G>A
  hgvsp: ENST00000567940.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+77G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.111G>A
  hgvsp: ENST00000569565.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-273G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.111G>A
  hgvsp: ENST00000573314.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+77G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+77G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+77G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+77G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-288G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+77G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+77G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys37Lys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/15-65903379-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903379
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903379
    reference: chr 15
allele count: 1
allele frequency: 8.431703204047218e-5
allele num: 11860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+57G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-293G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-308G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.91G>T
  hgvsp: ENSP00000454972.1:p.Val31Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-293G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.91G>T
  hgvsp: ENSP00000457977.1:p.Val31Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+57G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.91G>T
  hgvsp: ENSP00000458470.1:p.Val31Leu
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+57G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+57G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+57G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-308G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+57G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+57G>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-261G>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val31Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ

15-65903398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903398
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903398
    reference: chr 15
allele count: 6459
allele frequency: 5.258915486077186e-1
allele num: 12282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-327C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+38C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+38C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-280C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-312C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+38C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+38C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.72C>T
  hgvsp: ENST00000569565.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.72C>T
  hgvsp: ENST00000567940.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.72C>T
  hgvsp: ENST00000573314.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-327C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+38C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+38C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-312C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+38C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.25e1
  variant carriers: 306
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.75e1
  variant carriers: 725
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 5.25e1
  variant carriers: 616
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 497
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.75e1
  variant carriers: 191
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 2.25e1
  variant carriers: 78
genotype quality: GenotypeQuality
hgvs: p.Arg24Arg
num of homozygotes: 1768
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

15-65903400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903400
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903400
    reference: chr 15
allele count: 762
allele frequency: 6.199153921249593e-2
allele num: 12292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+36C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+36C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+36C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-314C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+36C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-314C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.70C>T
  hgvsp: ENSP00000458470.1:p.Arg24Cys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000379006
  ensembl transcript: ENST00000395644
  gene symbol: VWA9
  hgvsc: ENST00000395644.4:c.-329C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+36C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-329C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+36C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.70C>T
  hgvsp: ENSP00000457977.1:p.Arg24Cys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.70C>T
  hgvsp: ENSP00000454972.1:p.Arg24Cys
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+36C>T
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-282C>T
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 6.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 5.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 3.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
hgvs: p.Arg24Cys
num of homozygotes: 33
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-65903415-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903415
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903415
    reference: chr 15
allele count: 8
allele frequency: 6.503007641033978e-4
allele num: 12302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-329C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.55C>G
  hgvsp: ENSP00000458470.1:p.Pro19Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.55C>G
  hgvsp: ENSP00000457977.1:p.Pro19Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.55C>G
  hgvsp: ENSP00000454972.1:p.Pro19Ala
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+21C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+21C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-297C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+21C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-329C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+21C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-344C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+21C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+21C>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+21C>G
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro19Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

15-65903415-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903415
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903415
    reference: chr 15
allele count: 2
allele frequency: 1.625751910258494e-4
allele num: 12302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-329C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-329C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-297C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-63+21C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-63+21C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.51+21C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.51+21C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-157+21C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.55C>A
  hgvsp: ENSP00000458470.1:p.Pro19Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.55C>A
  hgvsp: ENSP00000457977.1:p.Pro19Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-46+21C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.57+21C>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.55C>A
  hgvsp: ENSP00000454972.1:p.Pro19Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-344C>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro19Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

15-65903442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903442
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903442
    reference: chr 15
allele count: 1
allele frequency: 8.124796880077999e-5
allele num: 12308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-69G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.28G>A
  hgvsp: ENSP00000457977.1:p.Ala10Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-356G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.45G>A
  hgvsp: ENST00000567923.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.45G>A
  hgvsp: ENST00000420799.2:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-163G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-356G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.28G>A
  hgvsp: ENSP00000458470.1:p.Ala10Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.51G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.28G>A
  hgvsp: ENSP00000454972.1:p.Ala10Thr
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-69G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-371G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-52G>A
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-324G>A
  variant of: http://identifiers.org/hgnc/25372
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala10Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

15-65903446-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903446
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903446
    reference: chr 15
allele count: 5
allele frequency: 4.061738424045491e-4
allele num: 12310
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsc: ENST00000420799.2:c.41A>G
  hgvsp: ENSP00000408429.2:p.Asp14Gly
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  hgvsc: ENST00000313182.2:c.-73A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  hgvsc: ENST00000431261.2:c.-167A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsc: ENST00000569565.1:c.24A>G
  hgvsp: ENST00000569565.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsc: ENST00000567923.1:c.41A>G
  hgvsp: ENSP00000454425.1:p.Asp14Gly
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsc: ENST00000567940.1:c.24A>G
  hgvsp: ENST00000567940.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  hgvsc: ENST00000569491.1:c.-56A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsc: ENST00000573314.1:c.24A>G
  hgvsp: ENST00000573314.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  hgvsc: ENST00000442903.3:c.-73A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  hgvsc: ENST00000568573.1:c.-375A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  hgvsc: ENST00000562830.1:c.-360A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  hgvsc: ENST00000561769.1:c.-328A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  hgvsc: ENST00000567744.1:c.-360A>G
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  hgvsc: ENST00000564306.1:n.47A>G
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Asp14Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

15-65903454-C-CACAGTCCGTCGGCATAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903454
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903471
    reference: chr 15
allele count: 1
allele frequency: 8.138020833333333e-5
allele num: 12288
alternate allele: CACAGTCCGTCGGCATAA
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsp: ENSP00000454972.1:p.Val6LeufsTer32
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsp: ENSP00000458470.1:p.Val6LeufsTer32
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsp: ENSP00000408429.2:p.Ser12TyrfsTer15
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsp: ENSP00000454425.1:p.Ser12TyrfsTer18
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsp: ENSP00000457977.1:p.Val6LeufsTer32
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser12TyrfsTer15
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum

15-65903457-A-AGTCCGTCGGCATAAACT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65903457
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 65903474
    reference: chr 15
allele count: 2
allele frequency: 1.627604166666667e-4
allele num: 12288
alternate allele: AGTCCGTCGGCATAAACT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457977
  ensembl transcript: ENST00000567940
  gene symbol: VWA9
  hgvsp: ENSP00000457977.1:p.Cys5SerfsTer33
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000396314
  ensembl transcript: ENST00000442903
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000138614
  ensembl transcript: ENST00000564306
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454425
  ensembl transcript: ENST00000567923
  gene symbol: VWA9
  hgvsp: ENSP00000454425.1:p.Ser12TyrfsTer18
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000408429
  ensembl transcript: ENST00000420799
  gene symbol: VWA9
  hgvsp: ENSP00000408429.2:p.Ser12TyrfsTer15
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456460
  ensembl transcript: ENST00000569491
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000456956
  ensembl transcript: ENST00000562830
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454743
  ensembl transcript: ENST00000561769
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000454972
  ensembl transcript: ENST00000569565
  gene symbol: VWA9
  hgvsp: ENSP00000454972.1:p.Cys5SerfsTer33
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000326379
  ensembl transcript: ENST00000313182
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457922
  ensembl transcript: ENST00000568573
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000402898
  ensembl transcript: ENST00000431261
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000458470
  ensembl transcript: ENST00000573314
  gene symbol: VWA9
  hgvsp: ENSP00000458470.1:p.Cys5SerfsTer33
  variant of: http://identifiers.org/hgnc/25372
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138614
  ensembl protein: ENSP00000457624
  ensembl transcript: ENST00000567744
  gene symbol: VWA9
  variant of: http://identifiers.org/hgnc/25372
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser12TyrfsTer15
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
reference allele: A

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

GenotypeDepth
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 315
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 607
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40518
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4584
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 911
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
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: 16490
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.69e-1

QD
type: SiteQuality
SIO_000300: 1.092e1

FS
type: SiteQuality
SIO_000300: 3.312e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.464447e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

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

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

African
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allele frequency: 9.619084263178146e-5
allele num: 10396
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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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

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

QD
type: SiteQuality
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 1.0e-4

MQRankSum
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ReadPosRankSum
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VQSLOD
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SIO_000300: -1.023e-1

ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.502195516524151e-3
allele num: 8654
num of homozygotes: 0

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

European (Non-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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QD
type: SiteQuality
SIO_000300: 1.255e1

VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 1.102e0

BaseQRankSum
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SIO_000300: -3.264e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 1.465942e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 3

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

European (Non-Finnish)
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allele num: 66716
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Finnish)
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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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.54e-1

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
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Other
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South Asian
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allele num: 16504
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66726
num of homozygotes: 0

Other
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African
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
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South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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QD
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MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 1.46899e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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FS
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
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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
allele num: 11570
num of homozygotes: 0

European (Finnish)
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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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South Asian
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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QD
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MQ
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BaseQRankSum
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FS
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SIO_000300: 4.106e0

ReadPosRankSum
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SIO_000300: 7.93e-1

DP
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SIO_000300: 1.469742e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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num of homozygotes: 0

European (Finnish)
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allele num: 6610
num of homozygotes: 0

East Asian
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South Asian
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Latino
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.25e-1

ClippingRankSum
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DP
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MQ
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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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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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num of homozygotes: 0

Latino
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Other
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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ClippingRankSum
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DP
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QD
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FS
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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South Asian
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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Other
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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FS
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MQ
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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FS
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InbreedingCoeff
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MQ
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DP
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QD
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European (Non-Finnish)
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African
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East Asian
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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MQRankSum
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ClippingRankSum
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FS
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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DP
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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FS
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QD
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East Asian
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DP
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MQ
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele num: 10402
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European (Finnish)
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allele count: 0
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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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allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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MQ
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SIO_000300: 6.0e1

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

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

Latino
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East Asian
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South Asian
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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MQ
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SIO_000300: 6.0e1

FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: 3.9e-3

ClippingRankSum
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SIO_000300: 5.36e-1

BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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allele frequency: 3.468007629616785e-4
allele num: 11534
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

African
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allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

Other
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European (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 count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
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InbreedingCoeff
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MQRankSum
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DP
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VQSLOD
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FS
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SIO_000300: 5.3e-1

QD
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 2.02e0

ClippingRankSum
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SIO_000300: -1.328e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

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

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

South Asian
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Other
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African
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East Asian
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InbreedingCoeff
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FS
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MQ
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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South Asian
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allele num: 16412
num of homozygotes: 0

European (Finnish)
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Latino
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Other
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East Asian
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MQ
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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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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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African
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South Asian
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Other
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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SIO_000300: 2.541e0

DP
type: SiteQuality
SIO_000300: 1.457428e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 7.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.04e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
allele frequency: 0.0e0
allele num: 66104
num of homozygotes: 0

East Asian
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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

African
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allele count: 2
allele frequency: 1.949697796841489e-4
allele num: 10258
num of homozygotes: 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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

FS
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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DP
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ClippingRankSum
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SIO_000300: -5.16e-1

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.901548869503294e-5
allele num: 11234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65528
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

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

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

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

ClippingRankSum
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SIO_000300: -1.04e0

BaseQRankSum
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SIO_000300: 1.56e-1

FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.56e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

QD
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ReadPosRankSum
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SIO_000300: 8.169999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

VQSLOD
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SIO_000300: -1.404e0

DP
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SIO_000300: 1.433836e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9644
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 5.075111652456354e-5
allele num: 59112
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele count: 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

MQRankSum
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InbreedingCoeff
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SIO_000300: -1.9e-3

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.744530895642162e-5
allele num: 57322
num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 57322
num of homozygotes: 0

East Asian
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European (Finnish)
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Latino
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Other
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VQSLOD
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QD
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ClippingRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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Latino
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Other
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South Asian
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allele frequency: 7.020499859590003e-5
allele num: 14244
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56300
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

BaseQRankSum
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SIO_000300: 6.31e0

DP
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QD
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VQSLOD
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InbreedingCoeff
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SIO_000300: -2.3e-3

FS
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MQRankSum
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SIO_000300: 1.59e0

MQ
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SIO_000300: 5.968e1

ClippingRankSum
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SIO_000300: -5.73e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.802776275464215e-5
allele num: 55470
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8768
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5366
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 2.077e0

InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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SIO_000300: -6.94e-1

QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.856320772229441e-5
allele num: 53870
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5210
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQRankSum
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VQSLOD
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FS
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QD
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: -5.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

MQ
type: SiteQuality
SIO_000300: 5.889e1

DP
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SIO_000300: 1.136096e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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variant carriers: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 7.485870419583037e-5
allele num: 53434
num of homozygotes: 0

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

African
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allele count: 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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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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: 2
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allele num: 44578
num of homozygotes: 0

Latino
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African
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Other
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European (Finnish)
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South Asian
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FS
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MQ
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VQSLOD
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ClippingRankSum
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QD
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

Other
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East Asian
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Latino
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African
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European (Finnish)
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South Asian
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QD
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BaseQRankSum
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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Other
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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FS
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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VQSLOD
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MQ
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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South Asian
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InbreedingCoeff
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DP
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MQRankSum
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FS
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QD
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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South Asian
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MQRankSum
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DP
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FS
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MQ
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VQSLOD
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QD
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MQ
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FS
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QD
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DP
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MQ
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African
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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East Asian
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Other
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European (Non-Finnish)
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allele num: 2730
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African
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South Asian
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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MQ
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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South Asian
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Other
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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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Latino
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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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European (Non-Finnish)
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ReadPosRankSum
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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MQ
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QD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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allele frequency: 0.0e0
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African
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Other
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InbreedingCoeff
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DP
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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num of homozygotes: 0

African
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Latino
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ClippingRankSum
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QD
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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East Asian
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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East Asian
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Latino
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African
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European (Finnish)
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South Asian
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InbreedingCoeff
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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QD
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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MQ
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VQSLOD
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FS
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DP
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Latino
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African
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East Asian
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European (Non-Finnish)
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FS
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VQSLOD
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DP
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MQ
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MQ
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VQSLOD
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GenotypeQuality
all individuals: 1894
bin: 7.5e0
variant carriers: 0

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

African
type: Population
allele count: 7
allele frequency: 1.325757575757576e-2
allele num: 528
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 6.024096385542169e-3
allele num: 166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5964
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2814
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.43e-2

FS
type: SiteQuality
SIO_000300: 2.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.882e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.21902e5

QD
type: SiteQuality
SIO_000300: 1.248e1

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

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

GenotypeDepth
all individuals: 295
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GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 1
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GenotypeDepth
all individuals: 66
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GenotypeQuality
all individuals: 3750
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 184
bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 62
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2187
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GenotypeQuality
all individuals: 286
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 244
bin: 8.25e1
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GenotypeQuality
all individuals: 771
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 66
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3442
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.360914534567229e-4
allele num: 7348
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.48659e5

VQSLOD
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

QD
type: SiteQuality
SIO_000300: 9.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.74e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 636
bin: 4.25e1
variant carriers: 616

GenotypeDepth
all individuals: 30
bin: 8.75e1
variant carriers: 30

GenotypeDepth
all individuals: 1634
bin: 2.5e0
variant carriers: 352

GenotypeDepth
all individuals: 66
bin: 9.75e1
variant carriers: 66

GenotypeDepth
all individuals: 381
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variant carriers: 378

GenotypeDepth
all individuals: 24
bin: 1.25e1
variant carriers: 14

GenotypeDepth
all individuals: 522
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variant carriers: 522

GenotypeDepth
all individuals: 283
bin: 6.75e1
variant carriers: 283

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 17

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 96

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 13

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 62

GenotypeQuality
all individuals: 931
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 215
bin: 6.75e1
variant carriers: 20

GenotypeQuality
all individuals: 1204
bin: 7.5e0
variant carriers: 217

GenotypeQuality
all individuals: 364
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 39

GenotypeQuality
all individuals: 120
bin: 8.25e1
variant carriers: 36

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 35

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 12

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 91
bin: 7.25e1
variant carriers: 15

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

GenotypeQuality
all individuals: 4563
bin: 9.75e1
variant carriers: 4541

GenotypeQuality
all individuals: 60
bin: 9.25e1
variant carriers: 36

GenotypeQuality
all individuals: 120
bin: 7.75e1
variant carriers: 26

GenotypeQuality
all individuals: 49
bin: 8.75e1
variant carriers: 23

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 3

South Asian
type: Population
allele count: 4138
allele frequency: 5.434725505647492e-1
allele num: 7614
num of homozygotes: 1141

European (Non-Finnish)
type: Population
allele count: 1546
allele frequency: 4.311210262130508e-1
allele num: 3586
num of homozygotes: 334

African
type: Population
allele count: 448
allele frequency: 8.0e-1
allele num: 560
num of homozygotes: 184

Latino
type: Population
allele count: 86
allele frequency: 4.623655913978494e-1
allele num: 186
num of homozygotes: 18

East Asian
type: Population
allele count: 169
allele frequency: 8.622448979591837e-1
allele num: 196
num of homozygotes: 74

Other
type: Population
allele count: 68
allele frequency: 5.151515151515151e-1
allele num: 132
num of homozygotes: 17

European (Finnish)
type: Population
allele count: 4
allele frequency: 5.0e-1
allele num: 8
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.84e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.64e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 2.229e1

DP
type: SiteQuality
SIO_000300: 2.78733e5

GenotypeDepth
all individuals: 80
bin: 7.75e1
variant carriers: 17

GenotypeDepth
all individuals: 510
bin: 2.75e1
variant carriers: 21

GenotypeDepth
all individuals: 2565
bin: 2.5e0
variant carriers: 29

GenotypeDepth
all individuals: 26
bin: 8.75e1
variant carriers: 6

GenotypeDepth
all individuals: 740
bin: 4.75e1
variant carriers: 116

GenotypeDepth
all individuals: 18
bin: 9.25e1
variant carriers: 3

GenotypeDepth
all individuals: 259
bin: 6.75e1
variant carriers: 56

GenotypeDepth
all individuals: 458
bin: 5.75e1
variant carriers: 75

GenotypeDepth
all individuals: 570
bin: 3.25e1
variant carriers: 51

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 331
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1060
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2399
bin: 7.5e0
variant carriers: 18

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 285
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3657
bin: 9.75e1
variant carriers: 734

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 2

African
type: Population
allele count: 48
allele frequency: 8.571428571428572e-2
allele num: 560
num of homozygotes: 4

South Asian
type: Population
allele count: 432
allele frequency: 5.670779732213179e-2
allele num: 7618
num of homozygotes: 23

Other
type: Population
allele count: 6
allele frequency: 4.545454545454546e-2
allele num: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 6.060606060606061e-2
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 5.913978494623656e-2
allele num: 186
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 253
allele frequency: 7.043429844097995e-2
allele num: 3592
num of homozygotes: 6

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

DP
type: SiteQuality
SIO_000300: 2.7185e5

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 7.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

QD
type: SiteQuality
SIO_000300: 1.728e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

GenotypeDepth
all individuals: 596
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2754
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 24
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variant carriers: 1

GenotypeDepth
all individuals: 20
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variant carriers: 0

GenotypeDepth
all individuals: 1004
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 638
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variant carriers: 2

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 237
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GenotypeQuality
all individuals: 3454
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variant carriers: 8

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

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 209
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GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 67
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 197
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GenotypeQuality
all individuals: 307
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GenotypeQuality
all individuals: 1121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 7.5e0
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GenotypeQuality
all individuals: 273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 6.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3602
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 1.049868766404199e-3
allele num: 7620
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.71e-2

MQ
type: SiteQuality
SIO_000300: 5.977e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

DP
type: SiteQuality
SIO_000300: 2.70744e5

QD
type: SiteQuality
SIO_000300: 1.339e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

GenotypeDepth
all individuals: 1004
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 20
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variant carriers: 0

GenotypeDepth
all individuals: 658
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
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variant carriers: 0

GenotypeDepth
all individuals: 577
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variant carriers: 0

GenotypeDepth
all individuals: 730
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GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
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GenotypeQuality
all individuals: 197
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GenotypeQuality
all individuals: 178
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variant carriers: 0

GenotypeQuality
all individuals: 209
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GenotypeQuality
all individuals: 3454
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 6.25e1
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 273
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 237
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variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 2.624671916010499e-4
allele num: 7620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.339e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.71e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

DP
type: SiteQuality
SIO_000300: 2.70744e5

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeDepth
all individuals: 658
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 444
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variant carriers: 0

GenotypeDepth
all individuals: 19
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GenotypeDepth
all individuals: 33
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GenotypeDepth
all individuals: 528
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GenotypeDepth
all individuals: 250
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GenotypeDepth
all individuals: 23
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GenotypeQuality
all individuals: 181
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 306
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 1146
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GenotypeQuality
all individuals: 239
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GenotypeQuality
all individuals: 2359
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GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 181
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 54
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GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 3450
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 354
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 1.312335958005249e-4
allele num: 7620
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.032e1

FS
type: SiteQuality
SIO_000300: 6.98e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.70546e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.031e0

MQRankSum
type: SiteQuality
SIO_000300: 4.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-2

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

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

GenotypeDepth
all individuals: 602
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 731
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 239
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 272
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3455
bin: 9.75e1
variant carriers: 5

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 8.928571428571428e-3
allele num: 560
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.81e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

DP
type: SiteQuality
SIO_000300: 2.7049e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.58e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.030000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.215e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.43e-1

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 530
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1998
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3446
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 306
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 6.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 1.314060446780552e-4
allele num: 7610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.448e0

MQ
type: SiteQuality
SIO_000300: 5.202e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.084e0

FS
type: SiteQuality
SIO_000300: 7.6e-1

QD
type: SiteQuality
SIO_000300: 3.54e0

DP
type: SiteQuality
SIO_000300: 2.69982e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-1

GenotypeDepth
all individuals: 364
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 731
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 578
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 181
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1972
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 240
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3447
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 353
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

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